NDC codes

FDA NDC Directory
Product NDC (as listed)43742-2184Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43742-2184Add 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 NDC11-digit (billing)PackageCopy
43742-2184-1437422184014374221840130 mL in 1 BOTTLE, DROPPER (43742-2184-1)Marketed from Aug 14, 2024

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)
adenosinum triphosphoricum dinatrum, bryonia (alba), cedron, dim (3, 3-diindolymethane), equol, faecalis (alkaligenes), ignatia amara, lachesis mutus, petroselinum sativum, sanguinaria canadensis, sepia, stannum metallicum, sulphur
Active ingredients
Adenosine triphosphate disodium — 6 [hp_X]/mLBryonia alba root — 8 [hp_X]/mLHomalolepis cedron seed — 12 [hp_X]/mL3,3'-diindolylmethane — 6 [hp_X]/mLEquol — 6 [hp_X]/mLAlcaligenes faecalis — 30 [hp_C]/mLStrychnos ignatii seed — 8 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLPetroselinum crispum whole — 6 [hp_X]/mLSanguinaria canadensis root — 3 [hp_X]/mLSepia officinalis juice — 4 [hp_X]/mLTin — 12 [hp_X]/mLSulfur — 6 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Labeler
Deseret Biologicals, Inc.NDC labeler code 43742
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 43742-2184_eae8a36a-2c73-47a6-9b31-e81cff8b61dcSPL ID eae8a36a-2c73-47a6-9b31-e81cff8b61dcSPL set ID 649d19e2-3bed-4d2e-834d-4354a90d87e6UNII 5L51B4DR1G, T7J046YI2B, KHI40967MV, SSZ9HQT61Z, 2T6D2HPX7Q, 05KB30NGW2, 1NM3M2487K, VSW71SS07I, 1WZA4Y92EX, N9288CD508, QDL83WN8C2, 387GMG9FH5, 70FD1KFU70UPC 0810151881874

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

N443742218401 followed by a unit qualifier and the quantity

Package 43742-2184-01. 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 .

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • menopausal support • hot flashes • mood swings • night sweats • flushing • headache • weakness • 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)

About NDC 43742-2184

What is NDC 43742-2184?
43742-2184 is the product NDC for Menopause Relief, Adenosine triphosphate disodium 6 [hp_X]/mL + 12 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Menopause Relief (Adenosinum Triphosphoricum Dinatrum, Bryonia (Alba), Cedron, DIM (3, 3-Diindolymethane), Equol, Faecalis (Alkaligenes), Ignatia Amara, Lachesis Mutus, Petroselinum Sativum, Sanguinaria Canadensis, Sepia, Stannum Metallicum, Sulphur).
What is the active ingredient?
Adenosine triphosphate disodium, Bryonia alba root, Homalolepis cedron seed, 3,3'-diindolylmethane, Equol, Alcaligenes faecalis, Strychnos ignatii seed, Lachesis muta venom, Petroselinum crispum whole, Sanguinaria canadensis root, Sepia officinalis juice, Tin, Sulfur.
Who is the labeler?
Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Menopause Relief?
3 other product NDCs are listed under this name. See all Menopause Relief NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Menopause Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Menopause Reliefamyl nit, calc carb, caulophyllum, cimicifuga, ferrum met, gelsemium, lachesis, pulsatilla, sanguinaria, sepia, sulphur and sulphuricum ac.Amyl nitrite 10 [hp_X]/59mL + 11 more ingredientsLiquidOralKing Bio Inc.57955-997357955-9973-02
Menopause Reliefsanguinaria canadensis, sepia, adenosinum triphosphoricum dinatrum, dim (3, 3-diindolymethane), equol, sulphur, petroselinum sativum, bryonia (alba), ignatia amara, cedron, lachesis mutus, stannum metallicum, faecalis (alkaligenes)Sanguinaria canadensis root 3 [hp_X]/mL + 12 more ingredientsLiquidOralDeseret Biologicals, Inc.43742-159043742-1590-01
Menopause Reliefbarium carbonate, atropa belladonna, black cohosh, nitroglycerin, lachesis muta venom, silicon dioxideBarium carbonate 10 [hp_X]/4g + 5 more ingredientsPelletSublingualHomeocare Laboratories61727-30861727-0308-21

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