Female Stimulant NDC 43742-1507

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1507Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1507Add 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
43742-1507-1	43742150701	30 mL in 1 BOTTLE, DROPPER (43742-1507-1)Marketed from Aug 20, 2019

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): lilium tigrinum, bovista, cypripedium pubescens, hydrastis canadensis, petroselinum sativum, aquilegia vulgaris, funiculus umbilicalis suis, glandula suprarenalis suis, heart (suis), kreosotum, oophorinum (suis), uterus (suis), folliculinum, lachesis mutus, magnesia phosphorica, mercurius solubilis, sepia, pineal gland (suis), hypophysis suis, aconiticum acidum cis-, apis venenum purum, estradiol, progesterone, testosterone, placenta totalis suis, faecalis (alkaligenes), mutabile bacillus (bach)
Active ingredients: Lilium lancifolium whole flowering — 4 [hp_X]/mLLycoperdon utriforme fruiting body — 6 [hp_X]/mLCypripedium parviflorum var. Pubescens root — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLPetroselinum crispum whole — 6 [hp_X]/mLAquilegia vulgaris — 8 [hp_X]/mLSus scrofa umbilical cord — 8 [hp_X]/mLSus scrofa adrenal gland — 8 [hp_X]/mLPork heart — 8 [hp_X]/mLWood creosote — 8 [hp_X]/mLSus scrofa ovary — 8 [hp_X]/mLSus scrofa uterus — 8 [hp_X]/mLEstrone — 8 [hp_X]/mLSus scrofa pituitary gland — 10 [hp_X]/mLAconitic acid, (Z)- — 10 [hp_X]/mLLachesis muta venom — 10 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLSepia officinalis juice — 13 [hp_X]/mLSus scrofa pineal gland — 16 [hp_X]/mLApis mellifera venom — 18 [hp_X]/mLEstradiol — 30 [hp_X]/mLProgesterone — 30 [hp_X]/mLTestosterone — 30 [hp_X]/mLSus scrofa placenta — 6 [hp_C]/mLAlcaligenes faecalis — 30 [hp_C]/mLEscherichia coli — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 20, 2019
Marketing end: Jan 2, 2030
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 43742-1507_98b646e4-e71f-46d3-9094-778235b7af46SPL ID 98b646e4-e71f-46d3-9094-778235b7af46SPL set ID 18d072ec-93e1-4e20-82db-98e80b81c363UNII X67Z2963PI, K2A74U428F, 21Y9GZ1LZA, ZW3Z11D0JV, 1WZA4Y92EX, 8POZ61U1G2, 118OYG6W3H, 398IYQ16YV, X876KJM95L, 3JYG22FD73, S7YTV04R8O, 2595C75F1P, 2DI9HA706A, L0PFEMQ1DT, OF5471ZHRR, VSW71SS07I, HF539G9L3Q, 324Y4038G2, QDL83WN8C2, 050QZ2EDK7, 76013O881M, 4TI98Z838E, 4G7DS2Q64Y, 3XMK78S47O, C8CV8867O8, 05KB30NGW2, 514B9K0L10UPC 0810151881393
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

N443742150701 followed by a unit qualifier and the quantity

Package 43742-1507-01. 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 May 27, 2025.

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)