Menopause Relief NDC 57955-9973

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9973Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9973Add 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
57955-9973-2	57955997302	59 mL in 1 BOTTLE, SPRAY (57955-9973-2)Marketed from Mar 13, 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): Menopause Relief
Generic name (nonproprietary): amyl nit, calc carb, caulophyllum, cimicifuga, ferrum met, gelsemium, lachesis, pulsatilla, sanguinaria, sepia, sulphur and sulphuricum ac.
Active ingredients: Amyl nitrite — 10 [hp_X]/59mLOyster shell calcium carbonate, Crude — 10 [hp_X]/59mLCaulophyllum thalictroides root — 10 [hp_X]/59mLBlack cohosh — 10 [hp_X]/59mLIron — 10 [hp_X]/59mLGelsemium sempervirens root — 10 [hp_X]/59mLLachesis muta venom — 10 [hp_X]/59mLPulsatilla vulgaris whole — 10 [hp_X]/59mLSanguinaria canadensis root — 10 [hp_X]/59mLSepia officinalis juice — 10 [hp_X]/59mLSulfur — 10 [hp_X]/59mLSulfuric acid — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 13, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 57955-9973_6fdc80e5-9b13-4bc0-b1da-305fdcb98463SPL ID 6fdc80e5-9b13-4bc0-b1da-305fdcb98463SPL set ID e12b75f5-6c5f-4b39-a6aa-dad07089f1d8UNII 22T8Z09XAK, 2E32821G6I, JTJ6HH6YEH, K73E24S6X9, E1UOL152H7, 639KR60Q1Q, VSW71SS07I, I76KB35JEV, N9288CD508, QDL83WN8C2, 70FD1KFU70, O40UQP6WCF

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

N457955997302 followed by a unit qualifier and the quantity

Package 57955-9973-02. 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 Mar 10, 2026.

Indications (excerpt from the label)

Uses † For temporary relief of discomforts associated with menopause: hot flashes night sweats chills headaches uterine cramps mood swings sensitivity irritability fatigue poor memory † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)