OHM Menopause NDC 66096-156

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-156Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0156Add 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
66096-156-05	66096015605	59 mL in 1 BOTTLE, SPRAY (66096-156-05)Marketed from Aug 19, 2015

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): OHM Menopause
Generic name (nonproprietary): ammonium carbonicum, amyl nitrosum, cimicifuga racemosa, glonoinum, lachesis mutus, sanguinaria, canadensis.
Active ingredients: Ammonium carbonate — 12 [hp_C]/59mLAmyl nitrite — 6 [hp_X]/59mLBlack cohosh — 3 [hp_X]/59mLNitroglycerin — 12 [hp_X]/59mLLachesis muta venom — 12 [hp_X]/59mLSanguinaria canadensis root — 4 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: OHM PHARMA INC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 19, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 66096-156_d44b458a-61ff-755e-e053-2995a90aebc0SPL ID d44b458a-61ff-755e-e053-2995a90aebc0SPL set ID 08dcc379-6d64-41b8-bf67-cab6031dcf72UNII NJ5VT0FKLJ, 22T8Z09XAK, K73E24S6X9, G59M7S0WS3, VSW71SS07I, N9288CD508UPC 0366096156053
Pharmacologic class: Nitrate Vasodilator

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

N466096015605 followed by a unit qualifier and the quantity

Package 66096-0156-05. 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 Dec 29, 2021.

Indications (excerpt from the label)

USES: Temporarily relieves symptoms caused by common menopause, hormonal imbalances. ** This statement has not been evaluated by the FDA. It is based on documented Homeopathic Materia Medica.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)