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DHEA Forte

NDC 43857-0052 · BioActive Nutritionals, Inc.

Generic nameDehydroepiandrosterone (DHEA), Pregnenolone, Progesterone,
Dosage formLIQUID
RouteORAL
Active ingredient(s)PRASTERONE, PREGNENOLONE, PROGESTERONE
Strength6; 6; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classProgesterone [CS], Progesterone [EPC]
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

43857-0052-1 — 30 mL in 1 BOTTLE, SPRAY (43857-0052-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0591-3128 — PROGESTERONE, 16714-157 — Progesterone, 16714-158 — Progesterone, 42291-784 — Progesterone, 42291-785 — Progesterone, 43598-349 — Progesterone, 43598-350 — Progesterone, 43742-0564 — DHEA (Dehydroepiandrosterone), 43742-0851 — Progesterone, 43857-0033 — Dehydroepiandrosterone, Estradiol, Pregnenolone, Progesterone, Testosterone, 43857-0084 — Progesterone, 43857-0103 — Progesterone, 43857-0120 — Progesterone, 43857-0166 — Dehydroepiandrosterone (DHEA), Estradiol, Hypophysis Suis, Pregnenolone, Progesterone, Spleen (Bovine), Testosterone, Thymus (Suis),…, 43857-0180 — Folliculinum, Progesterone, 43857-0284 — DHEA (Dehydroepiandrosterone) Pregnenolone, Progesterone, Testosterone, 44911-0047 — Progesterone, 50090-5928 — Progesterone, 50090-6475 — Progesterone, 50090-6771 — PROGESTERONE, +92 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.