NDC product
Female Stimulant
NDC 43742-2359 · Deseret Biologicals, Inc.
Key facts
| Product NDC | 43742-2359 |
|---|---|
| Proprietary name | Female Stimulant |
| 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) and 16 more |
| Substances | 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 and 15 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Deseret Biologicals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| DEA schedule | CIII |
| Pharmacologic classes | Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Calculi Dissolution Agent [EPC], Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA] and 10 more |
| Marketing start | Feb 19, 2026 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: