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Mescaline

Mescaline

 

What is Mescaline?

Mescaline is a psychedelic alkaloid that occurs naturally in the peyote cactus (Lophophora williamsii) and several other cactuses.  The chemical name for the drug is Mescaline hydrochloride or 3,4,5-trimethoxyphenethylaminehydrochloride.  The drug and peyote are illegal in the United States, and the drug is illegal in Canada. 

 

Native American tribes have used peyote for thousands of years during ceremonies and rituals.  Most of the Native American tribes are located in the southwestern United States and Mexico.  The drug has strong and intense hallucinogenic effects that can last for many hours. 

 

Overview of the Drug

Mescaline is produced naturally in Peyote, which is a small and spineless cactus.  The chemical is produced in the top of the cactus, called the “crown.”  The crowns are disc-like shapes and are cut off and eaten.  The drug is uncommon on the streets, and the majority of the drug is found on Native American reservations.  The drug is known as Buttons, Cactus, Mesc, and Peyoto on the streets. 

 

Method of Introduction

The drug can enter the body a couple of different ways.  The fresh or dried buttons of the cactus are usually chewed or soaked in water.  The cactus can also be ground down into a powder.  This powder can be placed in capsules or smoked in a leaf of cannabis or tobacco. 

 

A normal dosage of the drug is usually between 200 and 300 milligrams.  About 6 to 12 buttons are capable of producing the normal dosages, but consant users will need a higher dose because the body builds up a tolerance to the drug. 

 

Affects on the Mind

Mescaline is one of the strongest hallucinogenic substances.  It has affects that are similar to LSD, PCP, and psilocybin, and in some cases, the drug can produce more powerful hallucinations that the other two drugs.  Experiences with the drug differ from person to person, but common affects include powerful illusions and hallucinations along with an altered perception of time and space.  The drug can produce an altered body image or “out of body” experiences.  Feelings of euphoria and anxiety are common with this drug as well. 

 

Affect on the Body

Peyote and mescaline can cause serious side effects once they are ingested.  Common side effects include vomiting, serious nausea, a fast heart rate, increased blood pressure, a large amount of perspiration, a rise in body temperature, dilation of the pupils, muscle weakness, and headaches. 

 

Laws for Mescaline in the United States

Peyote and the drug are Schedule I substances in the United States under the Controlled Substances Act.  The drug is a Schedule I drug because it has a high risk of abuse, has not medical use in the United States, and is unsafe under medical supervision. 

 

Medical studies have examined the usefulness of peyote in the past, but not recent medical tests have examined the drug.  Other hallucinogenic drugs have been used in recent medical tests to treat depression, post traumatic stress disorder, and similar mental illnesses. 

 

Sources: https://www.justice.gov/dea/druginfo/drug_data_sheets/Peyote_Mescaline.pdf

Papaver Somniferum

Papaver Somniferum

 


What is Papaver somniferum?

 

Papaver somniferum is the scientific name for the poppy plant, which produces opium.  According to the Department of Justice, the plant was grown as early as 5,000 B.C. in the Mediterranean region.  There are several ways opium is derived from the poppy plant. 

 

One way to create opium is to gather the milky fluid that comes out of the seed pod and their air-dry the substance.  Pharmaceutical manufacturing extracts the alkaloids from a mature dried plant called a poppy straw. 

 

It is illegal to grow Papaver somniferum in the United States, and all pharmaceutical products are imported to United States from regulated areas abroad. 

 

Drug Facts from the Department of Justice

 

Opium is a Schedule II drug under the Controlled Substances Act.  Drugs with similar affects to opium include morphine, codeine, heroin, methadone, hydroquinone, fentanyl, and oxycodone.  These drugs produce similar effects because they are in the opiate family. 

 

Opium itself is found in a liquid form, solid form, or power form, but most illegal forms of opium come in a fine brown powder.  The drug can be smoked, injected intravenously, or taken as a pill.  According to the Department of Justice, opium is often abused along with other drugs.  A substance called “Black” is a mixture of opium, marijuana, and methamphetamine, while “Buddha” is opium and marijuana combined. 

 

Street names for opium include the following:

Ah-pen-yen, Aunti, Aunti Emma, Big O, Black pill, Chandoo, Chandu, Chinese Molasses, Chinese Tobacco, Dopium, Dover's Powder, Dream Gun, Dream Stick, Dreams, Easing Powder, Fi-do-nie, Gee, God's Medicine, Gondola, Goric, Great Tobacco, Guma, Hop/hops, Joy Plant, Midnight Oil, Mira, O, O.P., Ope, Pen Yan, Pin Gon, Pox, Skee, Toxy, Toys, When-shee, Ze, and Zero. 

 

Affects of the Drug on the Body

 

People used the drug derived from Papaver somniferum because of its euphoric effects on the mind.  The “high” experienced by opium is similar to the effects of heroin.  Depending on the method of administration, there is often an initial feeling of euphoria followed by relaxation and relief from pain. 

The drug is extremely addictive.  Some of the drugs first side effects on the body include constipation.  Additionally, the drug can cause the mouth and mucus membranes in the nose and sinuses to dry out.  Overdoses are common with opium because of its physical and psychological addictiveness.

Opium overdose effects include the following: slow breathing, dizziness, seizures, weakness, unconsciousness, coma, and even death. 

 

Legal Definitions Concerning Papaver somniferum

 

21 U.S.C. §802, also known as the Controlled Substances Act, defines narcotics drugs.  Subdivision (17) states the following: “The term “narcotic drug” means any of the following…(A) Opium, opiates, derivatives of opium and opiates, including their isomers, esters, ethers, salts, and salts of isomers, esters, and ethers, whenever the existence of such isomers, esters, ethers, and salts is possible within the specific chemical designations.  Such term does not include the isoquinoline alkaloids of opium…(B) Poppy straw and concentrate of poppy straw.”

 

Refer to the Controlled Substances Act for more information about opiates.

Sources: https://www.justice.gov/dea/druginfo/drug_data_sheets/Opium.pdf 

Eschscholzia Californica

Eschscholzia Californica

 


Eschscholzia Californica (California poppy or gold poppy)

 

Overview

 

Eschscholzia californica (California poppy or gold poppy) is the state flower of California.  According the Department of Agriculture, the plant grows in the Spring, Summer, and Fall and reaches a height of about 1.2 feet at maturity. 

 

The seeds of the plant can produce sedative-like feelings, but the poppy falls into a different class of alkaloids than poppies used in strong narcotics. 

The USDA states that the Eschscholzia californica (California poppy or gold poppy) is an invasive species.  Currently, the plant is found in Alaska, Alabama, Arizona, California, Colorado, Connecticut, Delaware, Georgia, Hawaii, Idaho, Kentucky, Louisiana, Maine, Michigan, Missouri, North Carolina, Nebraska, New Mexico, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Washington, Wisconsin, and Wyoming.  The plant is also found in six different parts of Canada. 

 

Legal Issues Connected to Eschscholzia californica (California poppy or gold poppy)

 

In some states, it is illegal to cut down the state flower regardless if it falls on public or private land.  However, it is not illegal to cut down the state flower in California unless it falls on public lands or along state or county roads. 

 

The law concerning the removal of the state flower, and any other plants for that matter, is referenced in California Penal Code Section 384a.  The penal code is paraphrased below:

 

“Every person who within the State of California willfully or negligently cuts, destroys, mutilates, or removes any tree or shrub, or fern or herb or build or cactus or flower, or huckleberry or redwood greens, or portion. . .growing upon state or county highway rights-of-way [excluding highway employees]. . .[or] growing upon public land or upon land not his or her own. . .is guilty of a misdemeanor and upon conviction thereof shall be punished by a fine or not more than one thousand dollars ($1,000), by imprisonment in a county jail for not more than six months, or by both fine and imprisonment.”

 

In order to cut down and/or remove plants and tree from private property, the owner of the property must provide written and signed consent to the person removing the plants.  The same applies on public lands.  In order to remove plants along public highways or on public land, the person or entity must receive written consent from the government body. 

 

Medicinal Uses of Eschscholzia californica (California poppy or gold poppy)

 

According to the Florida Museum of Natural History, Native Americans have used the plant throughout history as a cosmetic, to kill lice, and even relieve mild pain and treat insomnia.  As of 2005, there were still pharmacological studies concerning the plant according to the Florida Museum of Natural History. 

 

The plant is still used as a recreational drug in some circles, and the federal government does not control the use of the plant.  As mentioned before, the plant does have relaxing qualities if ingested, but the effects are mild compared to pharmaceutical opiates. 

 

Sources:

1. https://www.leginfo.ca.gov/cgi-bin/displaycode?section=pen&group=00001-01000&file=369a-402c

2. https://plants.usda.gov/java/profile?symbol=esca2

3. https://www.flmnh.ufl.edu/flowerpower/poppy.html  

Roll Your Own

Roll Your Own

 


What is a Roll-Your-Own Cigarette?

 

A roll-your-own cigarette (RYO) is a cigarette that is made with loose tobacco and a rolling paper.  RYO products often include a bag of loose tobacco, and these pouches sometimes come with rolling papers as well.

Some smokers preferred RYO products because they were cheaper and it allowed them to receive more nicotine than manufactured products on the market.  However, the cost of these products has sky rocketed in since 2009 after President Obama signed a piece of legislation that provided tax exemptions for RYO products.  The president also signed a piece of legislation in 2012 that end tax exemptions for manufacturers of RYO cigarettes. 

 

Increased Taxes on Roll-Your-Own Products Since 2009

 

In 2009, Congress expanded the State Children’s Health Insurance Program, and the expansion partly possible because the program raised taxes on cigarettes by 158 percent.  The tax went from $19.50 per thousand cigarettes to $50.33 per thousand cigarettes.  Congress expected consumers, and especially teenagers, to switch to roll-your-own products after the tax hike, so they hiked taxes on RYO products as well. 

 

The taxes on RYO products increased from $1.10 per pound to $24.78 per pound, an increase of 2,159 percent.  Taxes on small cigars increased as well, from $1.83 per thousand to $50.33 per thousand—an increase of 2,653 percent.  The tax hikes were strongly supported by the Campaign for Tobacco-Free Kids, the American Medical Association, the American Cancer Society, and the American Lung Association.

 

Since the take hikes, RYO sales have decreased by as much as 74%, but pipe tobacco sales have increased by more than 10%.  Here’s why.  Taxes on pipe tobacco only increased by 158%, and taxes on large cigars only increased by 155%.

 

Many manufacturers of RYO products began to advertise their products as pipe tobacco to avoid the tax increase.  There has also been an increase in commercial RYO machines that allow consumers to purchase tobacco and then place it in the machine that can role about 200 cigarettes in only a couple minutes.  These initiatives have allowed RYO manufacturers to avoid increased taxes, but President Obama signed a bill in 2012 that redefined tobacco manufacturers. 

 

Numerous Roll-Your-Own Cigarettes Stores Going Out of Business

 

On July 6, 2012, President Obama made a small amendment in the Federal Transportation Bill that redefined a tobacco manufacturer.  The bill states that any business with a RYO cigarette machine now classifies as a tobacco manufacturer and is subject to the same taxes for packaged cigarettes. 

The bill was signed after the Government Accountability Office save a huge increase in pipe tobacco sales.  The increase was due to increased taxes on RYO tobacco, so many consumers started using pipe tobacco in their rolled cigarettes because pipe tobacco was taxed less. 

 

The bill has caused several businesses to close their doors because the RYO cigarettes machines were expensive and the investment never paid for itself in time.  Opponents of the bill claim that consumers will still find a way to find cheap tobacco. 

Two Indicted for Shipping Illegal Meds into US

Two Indicted for Shipping Illegal Meds into US


On November 7, 2012, the Department of Justice reported that two Pakistani nationals were indicted by a federal grand jury in the District of Columbia for operating websites that shipped illegal pharmaceuticals into the United States from Pakistan and the United Kingdom.  The two defendants are Sheikh Waseem Ul Haq and Tahir Saeed.  


The indictment shows that Ul Haq and Saeed operated and owned Waseem Enterprises and Harry’s Enterprises in Pakistan.  The two men are believed to have shipped about $2 million of illegal pharmaceuticals around the world and about $780,000 to the United States.  


The two defendants made U.S. customers submit payments by Western Union to people in Karachi, Pakistan so they could conceal the funds.  They also told U.S. citizens that U.S. customs officials may intercept the packages as they enter the United States.  


The illegal drugs include the following:


•    alprazolam (labeled as Xanex)
•    diazepam (labeled as Valium)
•    lorazepam (labeled as Ativan)
•    clonazepam (labeled as Klonapin)
•    numerous types of anabolic steroids and other controlled substances


The defendants are charged with conspiring to import illegal pharmaceuticals to the United States, conspiring to distribute controlled substances, conspiracy to using misbranded pharmaceuticals, importing and distributing controlled substances, and conspiracy to commit money laundering.  


The two defendants each face 20 years in prison for each count of the importing and exporting conspiracy, as well as 20 years in prison for the money laundering charge.  They face more time with other charges as well.  


Stuart F. Delery, Acting Assistant Attorney General for the Civil Division, stated: “This prosecution aims to curb the flow of dangerous drugs into the hands of United States citizens.  The drugs allegedly sold by the defendants were not approved for distribution in the United States, were not dispensed by U.S. licensed pharmacies, and were not prescribed by any physician.”


Source: Federal Bureau of Investigation
 

Xarelto Approved to Treat and Reduce Blood Clots

Xarelto Approved to Treat and Reduce Blood Clots


On November 2, the Food and Drug Administration (FDA) approved Xarelto (rivaroxaban) to treat deep vein thrombosis (DVT) and pulmonary embolisms (PE), as well as to reduce the risk of DVT and PE after a surgery or treatment.  


DVT is a serious type of clot that occurs when blood thickens in a deep vein of the body.  These types of clots are most common in the lower leg and the thigh and are extremely dangerous if they break off.  They can travel to an artery in the lungs and can restrict blood flow—possibly leading to the PE which is deadly.  


The drug was already approved by the FDA and used after knee and hip replacement surgeries.  The drug was also used to reduce the risk of stroke in people with an irregular heartbeat called non-valvular atrial fibrillation.  


Richard Pazdur, M.D., states: “Xarelto is the first oral anti-clotting drug approved to treat and reduce the recurrence of blood clots since the approval of warfarin nearly 60 years ago.  Pazdur is the director of the Office of Hematology and Oncology Products at the Drug Evaluation and Research Center for the FDA.  


Other drugs that are approved to reduce the risk of blood clots include the following: Lovenox (enoxaparin), generic enoxaparin, Arixtra (fondaparinux), Fragmin (dalteparin), Coumadin (warfarin), and heparin.  


In clinical studies, only about 2.1 percent of patients taking Xarelto and 1.8 percent to 3 percent of patients taking enoxaparin and other combinations had a recurrent DVT or PE.  A specific study showed that 1.3 percent of patients taking Xarelto had a recurrent DVT or PE compared to 7.1 percent of patients taking a placebo.  


The main side effect of Xarelto is bleeding or uncontrolled bleeding.  These side effects are common with anti-clotting medicine.  


Source: U.S. Food and Drug Administration

Leader of Indianapolis Drug Organization Gets 10 Years

Leader of Indianapolis Drug Organization Gets 10 Years


On November 7, 2012, Immigration and Customs Enforcement (ICE) announced that Agustin Lozano was sentenced to 10 years in prison for leading a drug trafficking organization that ran drugs between Mexico and Chicago.  The investigation was led by ICE’s Homeland Security Investigations (HSI), the DEA, the IRS’s Criminal Investigation Division, and the Indianapolis Metro Drug Task Force.  


Lozano is a Mexican national, and he was sentenced on November 6, 2012 before U.S. District Judge William T. Lawrence with the Southern District of Indiana.  Lozano pleaded guilty to drug trafficking and money laundering, and he’ll be turned over to the ICE after he serves his prison sentence to face deportation.  


Starting in July of 2010, undercover agents started working with Lozano.  An undercover agent bought three grams of cocaine for $150 initially.  It took eight months to coordinate the investigation and gather information between agencies, and 48 kilograms of cocaine were eventually confiscated on December 15, 2010.  The cocaine had an estimated street value of $1.5 million.  Authorities confiscated 4.4 pounds of methamphetamine as well.  The methamphetamine had an estimated street value of $80,000.  


Throughout the investigation, it was found that the criminal organization distributed about five pounds of methamphetamine and 10 kilos of cocaine throughout Indianapolis every month.  184 pounds of marijuana, $69,500 in cash, and 18 firearms were confiscated during the investigation as well.  


U.S. Attorney Joseph H. Hogsett stated, “This sentence is an example of proactive and cooperative anti-drug police work at its finest.  A drug bust of this significance occurs only once every couple of years.  Let the message be heard loud and clear to all those who seek mayhem by trafficking in illegal narcotics – you will be identified, you will be investigated and you will be prosecuted to the fullest extent of the law.”


Source: U.S. Immigration and Customs Enforcement

Advair Diskus 250 50 Price

Advair Diskus 250 50 Price

A Brief Overview of the Advair Diskus 250 50 price

Patients with respiratory conditions such as emphysema or asthma may be prescribed Advair Diskus. Although expensive, several pricing options must be considered to achieve a lower Advair 250 50 price.

Before prescribing this medication, a physician's office will contact your insurance company if you are uncertain as to whether your policy can cover part or all of the Advair Diskus 250 50 price. Depending on your policy, the total cost incurred by the Advair 250 50 price may be covered completely or up to a certain point. If you suffer from asthma, keep in mind that this drug is only indicated for short-term use. Therefore, you may be able to determine the final bill for a fixed course of treatment after learning what the Advair Diskus 250 50 price is from a trusted provider.

While patients who live in an area with multiple pharmacies may be quoted more than one Advair 250 50 price, these may not be low enough to fit their budget. Likewise, patients in rural areas  may wish to shop online to locate a pharmacy which lists its Advair Diskus 250 50 price. Buying medication online is not a process to be undertaken casually. Consult with your physician to see if they are aware of any reputable online pharmacy which may list a suitable Advair 250 50 price.

No matter how low the listed Advair Diskus 250 50 price, do not purchase medication from any online pharmacy which does not require a prescription to make a sale. Websites which offer Advair 250 50 price without a prescription are not operating in accordance with the law. Because they have already demonstrated a willingness to break the law, they cannot be trusted with your credit card information.

To help decrease the Advair Diskus 250 50 price, the manufacturer is currently offering a coupon which removes $10 from every monthly purchase. This coupon to lower the Advair 250 50 price must be printed out and presented along with a prescription at a pharmacy. Additionally, at this time the manufacturer is currently offering a free 30-day trial dose to patients with a prescription. Such offers of assistance in lowering the Advair Diskus 250 50 price are constantly changing and contain many restrictions. You should also ask your doctor if they have any coupons which can lower the Advair 250 50 price.

You should be confident that you are receiving what you paid for regardless of the Advair Diskus 250 50 price. If medication you purchase turns out to be incorrectly dosed or otherwise defective, a pharmacy may be liable for damages if adverse effects ensue. Maintain receipts of any purchase recording the Advair 250 50 price paid. These will be necessary for a lawyer to determine how much compensation you should seek if litigation is likely to result in success.

 

Fen-Phen

Fen-Phen

What is Fen-Phen?
 
 
Fen-Phen is a drug combination that consists of fenfluramine and pherntermine and was used to treat obesity. It has since been withdrawn from the market. At first, the drug was found to be useful against obesity and hailed as a “diet miracle”, although patients were found to relapse after stopping treatment. Eventually the drug was found largely ineffective at helping weight loss, only improving the mood of the patient and increasing dependency on a mood altering medication.
 
 
How does Fen-Phen work?
 
 
Fenfluramine releases more serotonin into the body, tricking the body into feeling full. The downside is that the increase in serotonin has cause psychotic episodes and other undesirable mental disorders. Adding pherntermine to the fenfluramine was thought to counteract the harmful psychological effects of serotonin imbalance and this drug combination was done “off label” or unapproved by the Food and Drug Administration. Fen-Phen was intended to affect the serotonin receptor that made the patient feel full, but it also stimulated another receptor that led to problems with the heart. This is known as neurotoxcity and was unaccounted for in studies about the affect Fen-Phen has on the body.
 
 
What are the risks associated with taking Fen-Phen?
 
 
There were early indications that fenfluramine caused pulmonary hypertension or the thickening of the lungs that in turn affects proper breathing. Nonetheless, a variation of the drug, brand named Redux was approved and sold to American consumers until the FDA announced its withdrawal in 1997. There were additional concerns about the effect of the drug on heart valves with as many as 66 cases of disease in patients that had been taking fenfluramine and its variants.
 
 
What has been the liability, assessed to date?
 
 
Wyeth pharmaceuticals (now owned by Pfizer), the distributor of fenfluramine and Redux has an estimated liability of 14 billion owed to individuals that have suffered from taking Fen-Phen. There has been dispute as to the amount of individuals affected by cardiac distress by this drug with some estimates ranging as high as thirty percent. Studies have shown that individuals that have taken this drug for more than two years have a 17% increased chance of developing heart valve disease.
 
 
What should I do if I have been negatively impacted by this drug?
 
 
An electrocardiogram from a licensed healthcare provider is essential to failing a claim for your share of the settlement. Disbursement of compensation had slowed after falsified or misleading electrocardiograms were submitted for claims by doctors that were paid by law firms. An attorney can better help you determine if you are eligible for damages due to medical expenses, loss of wages and pain and anguish.
 
 
 

Pure Food and Drug Act

Pure Food and Drug Act

 
 
 
 
What is the Pure Food and Drug Act?
 
 
The Pure Food and Drug act of 1906 is a federal law that mandates for the inspection of meat products and forbids the sales, manufacturing or transportation of poisonous patent medicines and adulterated food products. The Pure Food and Drug Act was the first of more than 200 federal laws that constitute one of the world’s most inclusive and operative networks of consumer protections and public health concerns. 
 
 
The purpose of the Pure Food and Drug Act was to protect the American public from products identified as healthy without a scientific basis or support. The act also aimed to protect against the adulteration of food; the act was implemented to curb the spread of disease and food-induced illnesses. 
 
 
The Pure Food and Drug Act aimed to clean-up the American food and drug industry. At the turn of the 20th century, America’s food supply was enshrouded in unsafe and disgusting practices. Diseases were rampant as American slaughter and packing houses were not regulated nor checked for sanitation purposes. At this time there were now laws permitting the government to inspect these hubs and food processing plants. As a result, these filthy stations processed and packaged food, then shipped the product throughout the country. The end result 
 
 
What Sparked the Passing of the Pure Food and Drug Act?
 
 
The Pure Food and Drug Act aimed to clean-up the American food and drug industry. At the turn of the 20th century, America’s food supply was enshrouded in unsafe and disgusting practices. Diseases were rampant as American slaughter and packing houses were not regulated nor checked for sanitation purposes. At this time there were now laws permitting the government to inspect these hubs and food processing plants. As a result, these filthy stations processed and packaged food then shipped the product throughout the country. The result was the delivery of an unsanitary and potentially deadly food product. 
 
 
A heightened Public awareness during the early 20th century regarding the issues surrounding careless food preparation and the growing rate of drug addictions from patent medicines influenced government to create and subsequently pass the “Pure Food and Drug Act of 1906.” 
 
 
Although the public outcry was substantial, this fervency was sparked by federal employees. Individuals, such as Dr. Harvey Wiley (Chief Chemist for the Department of Agriculture) published findings on the widespread use of malignant preservatives used in food preparation and the meat-packing industry. These findings were accelerated by the “embalmed beef” disaster imposed on American Soldiers during the Spanish-American War—a violent outbreak that killed thousands of troops. 
 
 
The foundation of the Pure Food and Drug Act was promulgated by Theodore Roosevelt. The President began the process of implementing food and drug safety protocols by ensuring the passages of preceding legislation, including the Meat Inspection Act of 1906. These laws built the frameworks for the Pure Food and Drug Act.
 
 
What did the Pure Food and Drug Act of 1906 Enforce?
 
 
The Food and Drug Act of 1906 was applied to all food products shipped in foreign or interstate commerce. The purpose of the Food and Drug Act was to eliminate misbranding or adulteration from occurring.
 
 
The Federal Government defined alteration in the following ways: for confectionary products, adulteration occurred when the product yields any mephitic or poisonous colors, flavors or any ingredients that are regarded as harmful. Food products were considered adulterated if the good contained decomposed or filthy animal matter or byproduct. Food was also labeled as adulterated if the product contained deleterious ingredients, was poisonous or was comprised of inferior components. 
 
 
The Pure Food and Drug Act of 1906 contained the following provisions:
 
 
The Pure Food and Drug Act of 1906 required all drugs to be shipped and stored on commercial shelves with clearly-readable warning labels. These warnings labels must notify the user of any habit-forming drugs within the product or any damaging side effects.
 
 
The Pure Food and Drug Act of 1906 required that all prescriptions be supplied and affirmed only by licensed physicians. If the prescription was not given by a licensed physician the patient would be disallowed from purchasing the said drug.
 
 
The Pure Food and Drug Act of 1906 prohibited the delivery of diseased or otherwise rotten food in interstate and foreign commerce. The Act also barred the use of spoiled vegetable and animal products. Food was not to be delivered with substituted ingredients that would irritate or add harmful ingredients. In terms of drugs, the Pure Food and Drug Act of 1906, enabled government to seized any drugs or offending bodies that violated the warning sign stipulations of the act. 
 
 
 
The Pure Food and Drug Act created the Food and Drug Administration. Absolutely its most notable provision, the creation of the Food and Drug Administration established a government agency that was responsible for the testing of all foods and drugs used for human consumption. 
 
 
Facts about the Food and Drug Administration:
 
 
Currently operating within the United States Department of Health and Human Services, the Food and Drug Administration, is responsible for promoting and protecting public health through the supervision and regulation of food safety, tobacco products, prescription drugs, dietary supplements, vaccines, over-the-counter pharmaceutical drugs, cosmetics, medical devices, biopharmaceuticals, electromagnetic radiation emitting devices, vaccines and veterinary products. 
 
 
The Food and Drug Administration, in addition to regulating the aforementioned products, enforces various laws to promote the safe consumption of food and legal drugs. To accomplish its goal, the FDA, enforces Section 361 of the Public Health Service Act, which institutes a series of regulations and requirements concerning the sanitation of said products, particularly how they are shipped and stored. Through their enforcement capabilities, the Food and Drug Administration aims to control the spread of outbreak and food-related illness.