Fem Pro Drops

NDC 63083-2025 · Professional Complementary Health Formulas

Generic nameFem Pro Drops

Dosage formLIQUID

RouteORAL

Active ingredient(s)CHASTE TREE FRUIT, CAULOPHYLLUM THALICTROIDES ROOT, BLACK COHOSH, RUBUS IDAEUS FRUIT VOLATILE OIL, BOS TAURUS PITUITARY GLAND, POSTERIOR, BETA-ENDORPHIN HUMAN, ESTROGENS, CONJUGATED, PROGESTERONE

Strength30; 6; 12; 6; 3; 30; 30; 6 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL

Pharmacologic classEstrogen Receptor Agonists [MoA], Estrogen [EPC], Estrogens, Conjugated (USP) [CS], Progesterone [CS], Progesterone [EPC]

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

63083-2025-2 — 59 mL in 1 BOTTLE, DROPPER (63083-2025-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

61657-2969 — Adrenalinum, Cimicifuga, Ignatia, Lecithin, Nicotinamidum, Oophorinum, Sepia., 61727-308 — BARIUM CARBONATE, ATROPA BELLADONNA, BLACK COHOSH, NITROGLYCERIN, LACHESIS MUTA VENOM, SILICON DIOXIDE, 62106-0117 — Aconitum napellus, Cimicifuga racemosa, Lachesis mutus, Melissa officinalis, Platinum metallicum, Sanguinaria canadensis, Sepia,…, 62106-0623 — Apis mellifica, Belladonna, Caulophyllum thalictroides, Cimicifuga racemosa, Dioscorea villosa, Gelsemium sempervirens, Helonias dioica,…, 62185-0050 — Acetaldehyde, Dopamine Hydrochloride, DHEA (Dehydroepiandrosterone), 7-Oxo-Dehydroepiandrosterone-3B-Acetate, Folliculinum, Oophorinum…, 63083-1517 — Estrogen, 63083-1538 — Progesterone, 63083-2007 — Anti-Smoking I Drops, 63083-2008 — Anti-Smoking II Drops, 63083-2015 — Melancholy Drops Extrovert, 63083-2029 — Hyperthyroid Drops, 63083-2044 — Menopause Drops, 63083-2063 — Substance Abuse Drops, 63083-2072 — Tinnitus Drops, 63083-2124 — PMS Drops, 63083-2138 — Dysfunctional Bleeding Drops, 63083-2149 — Lactation Flow Drops, 63083-2151 — Varicose Vein Drops, 63083-2160 — Growth Hormone Drops, 63083-2171 — Difficulty Breathing Drops, +370 more

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