Female Stimulant NDC 43742-2359

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2359Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2359Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
43742-2359-1	43742235901	30 mL in 1 BOTTLE, DROPPER (43742-2359-1)Marketed from Feb 19, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Female Stimulant
Generic name (nonproprietary): 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)
Active ingredients: Aconitic acid, (Z)- — 20 [hp_X]/mLApis mellifera venom — 18 [hp_X]/mLAquilegia vulgaris — 8 [hp_X]/mLLycoperdon utriforme fruiting body — 6 [hp_X]/mLCypripedium parviflorum var. Pubescens root — 6 [hp_X]/mLEstradiol — 30 [hp_X]/mLAlcaligenes faecalis — 30 [hp_C]/mLEstrone — 8 [hp_X]/mLSus scrofa umbilical cord — 8 [hp_X]/mLSus scrofa adrenal gland — 8 [hp_X]/mLPork heart — 8 [hp_X]/mLGoldenseal — 6 [hp_X]/mLSus scrofa pituitary gland — 13 [hp_X]/mLWood creosote — 8 [hp_X]/mLLachesis muta venom — 10 [hp_X]/mLLilium lancifolium whole flowering — 4 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/mLMercurius solubilis — 10 [hp_X]/mLEscherichia coli — 30 [hp_C]/mLSus scrofa ovary — 8 [hp_X]/mLPetroselinum crispum whole — 6 [hp_X]/mLSus scrofa pineal gland — 12 [hp_X]/mLSus scrofa placenta — 6 [hp_C]/mLProgesterone — 30 [hp_X]/mLSepia officinalis juice — 10 [hp_X]/mLTestosterone — 30 [hp_X]/mLSus scrofa uterus — 8 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 19, 2026
Listing expires: Dec 31, 2027
DEA schedule: CIII
Other FDA classes: Androgen Receptor Agonists (Mechanism)Androstanes (Chemical structure)Estradiol Congeners (Chemical structure)Estrogen Receptor Agonists (Mechanism)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Progesterone (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43742-2359_654dd151-c2ca-4992-a17e-246d9752370cSPL ID 654dd151-c2ca-4992-a17e-246d9752370cSPL set ID 0d4b8cbf-8f57-43ca-a904-c69d9056c865UNII OF5471ZHRR, 76013O881M, 8POZ61U1G2, K2A74U428F, 21Y9GZ1LZA, 4TI98Z838E, 05KB30NGW2, 2DI9HA706A, 118OYG6W3H, 398IYQ16YV, X876KJM95L, ZW3Z11D0JV, L0PFEMQ1DT, 3JYG22FD73, VSW71SS07I, X67Z2963PI, HF539G9L3Q, 324Y4038G2, 514B9K0L10, S7YTV04R8O, 1WZA4Y92EX, 050QZ2EDK7, C8CV8867O8, 4G7DS2Q64Y, QDL83WN8C2, 3XMK78S47O, 2595C75F1P
Pharmacologic class: Androgen; Calculi Dissolution Agent; Estrogen; Osmotic Laxative; Progesterone

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443742235901 followed by a unit qualifier and the quantity

Package 43742-2359-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Feb 19, 2026.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • female support • fatigue • low sex drive These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)