Menopause Relief NDC 43742-1590

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1590Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1590Add 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
43742-1590-1	43742159001	30 mL in 1 BOTTLE, DROPPER (43742-1590-1)Marketed from Nov 14, 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): Menopause Relief
Generic name (nonproprietary): sanguinaria canadensis, sepia, adenosinum triphosphoricum dinatrum, dim (3, 3-diindolymethane), equol, sulphur, petroselinum sativum, bryonia (alba), ignatia amara, cedron, lachesis mutus, stannum metallicum, faecalis (alkaligenes)
Active ingredients: Sanguinaria canadensis root — 3 [hp_X]/mLSepia officinalis juice — 4 [hp_X]/mLAdenosine triphosphate disodium — 6 [hp_X]/mL3,3'-diindolylmethane — 6 [hp_X]/mLEquol, (-)- — 6 [hp_X]/mLSulfur — 6 [hp_X]/mLPetroselinum crispum — 6 [hp_X]/mLBryonia alba root — 8 [hp_X]/mLStrychnos ignatii seed — 8 [hp_X]/mLSimaba cedron seed — 11 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLTin — 12 [hp_X]/mLAlcaligenes faecalis — 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: Nov 14, 2019
Marketing end: Dec 5, 2028
Identifiers: Product ID 43742-1590_6e465431-8fda-4058-9a98-4dc320d34733SPL ID 6e465431-8fda-4058-9a98-4dc320d34733SPL set ID 802e3090-79fe-4daa-8b03-5843e33f6978UNII N9288CD508, QDL83WN8C2, 5L51B4DR1G, SSZ9HQT61Z, 2T6D2HPX7Q, 70FD1KFU70, 1WZA4Y92EX, T7J046YI2B, 1NM3M2487K, KHI40967MV, VSW71SS07I, 387GMG9FH5, 05KB30NGW2

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

N443742159001 followed by a unit qualifier and the quantity

Package 43742-1590-01. 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 Aug 14, 2024.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to hormone fluctuations associated with menopause, including hot flashes, mood swings, night sweats, flushing, headache, weakness, and lack of energy.** **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)