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napsgear
genezapharmateuticals
domestic-supply
puritysourcelabs
UGL OZ
UGFREAK
napsgeargenezapharmateuticals domestic-supplypuritysourcelabsUGL OZUGFREAK

Sketchy as hell

yes def. looks ugl or homebrew to me. that label looks made on a home computer printer ?

then again i cant enlarge the pic
 
Def homebrew, but labels do not necessarily mean the product is crap. I for one have used products made with THEE shittiest inkjet printers. Its inside is what counts, regarding your question. Cottonseed oil is yellow. Test E/C are usually clear and light yellow. Not a plat so I cannot englarge.
 
just be careful with ugl bro.Dont start shooting just anything, you can get nasty infections if its not clean gear.
 
Infections are no fun at all. Never had them, but have know those who have and it isn't pretty.
 
just be careful with ugl bro.Dont start shooting just anything, you can get nasty infections if its not clean gear.

If its not Human grade, or Vet...its UGL. Period. Fancy name, fancy label, whatever....you dont know if its made in a kitchen sink or a lab....its all UGL if it aint pharmacuetical.

People are creating a fallacy by trying to allude that brand x is not UGL.

Here is a simple description of what the FDA requires...somehow I dont think that any test pictured here in the gear picture section went through this process....therefore they are all UGL

Development & Approval Process (Drugs)


American consumers benefit from having access to the safest and most advanced pharmaceutical system in the world.
The main consumer watchdog in this system is the U.S. Food and Drug Administration's Center for Drug Evaluation and Research (CDER). The center's best-known job is to evaluate new drugs before they can be sold. The center's evaluation not only prevents quackery, but also provides doctors and patients the information they need to use medicines wisely. CDER ensures that drugs, both brand-name and generic, work correctly and that their health benefits outweigh their known risks.
Drug companies seeking to sell a drug in the United States must first test it. The company then sends CDER the evidence from these tests to prove the drug is safe and effective for its intended use. A team of CDER physicians, statisticians, chemists, pharmacologists, and other scientists reviews the company's data and proposed labeling. If this independent and unbiased review establishes that a drug's health benefits outweigh its known risks, the drug is approved for sale. The center doesn't actually test drugs itself, although it does conduct limited research in the areas of drug quality, safety, and effectiveness standards.
Before a drug can be tested in people, the drug company or sponsor performs laboratory and animal tests to discover how the drug works and whether it's likely to be safe and work well in humans. Next, a series of tests in people is begun to determine whether the drug is safe when used to treat a disease and whether it provides a real health benefit.
 
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