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After more than a hundred people, including many children, died across fifteen states, Congress passed the Federal Food, Drug, and Cosmetic Act of 1938, which authorized the F.D.A
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Product Details Active Ingredient : Bremelanotide (PT-141) Concentration : 20 mg per vial (lyophilized powder) Administration : Subcutaneous injection after reconstitution Volume : Reconstituted per provider instruction (typically 12 mL bacteriostatic water) Use : For clinical and research use under medical supervision Storage : Store lyophilized powder at 28C (3646F)
The procedure is simple, usually given as an injection or IV drip, similar to a routine shot
