Does HGH Therapy have approval from the FDA?
Congress passed the Dietary Supplement Health and Education Act in 1994 also known as (DSHEA-1994). DSHEA created a new food category for dietary supplements. In order for the FDA to remove a dietary supplement from the market, it must prove that the product causes undue harm to the consumers. DSHEA allows for low dose hormones in the form of Gels, Creams, Transdermal Patches, or capsules (Estrogen, Progesterone, HCG, DHEA, Melatonin, etc.) to be sold and marketed as dietary supplements. When delivered using a safe method of administration (sub-lingual, a tablet, capsule, cream, gel, etc.), bioidentical hormones fall into the category of foods, not drugs. FDA Overview of Dietary Supplements: http://www.cfsan.fda.gov/~dms/ds-oview.
