Female Stimulant

Product NDC

43742-2359

11-digit product format

437422359

Labeler code

43742

Product ID

43742-2359_654dd151-c2ca-4992-a17e-246d9752370c

Type

HUMAN OTC DRUG

Nonproprietary name

Aconiticum Acidum, Cis-, Apis Venenum Purum, Aquilegia Vulgaris, Bovista, Cypripedium Pubescens, Estradiol, Faecalis (Alkaligenes), Folliculinum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Heart (Suis), Hydrastis Canadensis, Hypophysis Suis, Kreosotum, Lachesis Mutus, Lilium Tigrinum, Magnesia Phosphorica, Mercurius Solubilis, Mutabile Bacillus (Bach), Oophorinum (Suis), Petroselinum Sativum, Pineal Gland (Suis), Placenta Totalis Suis, Progesterone, Sepia, Testosterone, Uterus (Suis)

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2026-02-19

Substance

ACONITIC ACID, (Z)-; APIS MELLIFERA VENOM; AQUILEGIA VULGARIS; LYCOPERDON UTRIFORME FRUITING BODY; CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT; ESTRADIOL; ALCALIGENES FAECALIS; ESTRONE; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PORK HEART; GOLDENSEAL; SUS SCROFA PITUITARY GLAND; WOOD CREOSOTE; LACHESIS MUTA VENOM; LILIUM LANCIFOLIUM WHOLE FLOWERING; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MERCURIUS SOLUBILIS; ESCHERICHIA COLI; SUS SCROFA OVARY; PETROSELINUM CRISPUM WHOLE; SUS SCROFA PINEAL GLAND; SUS SCROFA PLACENTA; PROGESTERONE; SEPIA OFFICINALIS JUICE; TESTOSTERONE; SUS SCROFA UTERUS

Active strength

20; 18; 8; 6; 6; 30; 30; 8; 8; 8; 8; 6; 13; 8; 10; 4; 10; 10; 30; 8; 6; 12; 6; 30; 10; 30; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Pharmacologic classes

Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Calculi Dissolution Agent [EPC], Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Progesterone [CS], Progesterone [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

DEA schedule

CIII

NDC exclude flag

No

Listing certified through

2027-12-31

Current FDA listing

Yes