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Menstrual Relief

NDC 36800-979 · Topco Associates, LLC

Generic nameAcetaminophen, Pamabrom, Pyrilamine maleate
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, PAMABROM, PYRILAMINE MALEATE
Strength500; 25; 15 mg/1; mg/1; mg/1
Marketing categoryOTC MONOGRAPH DRUG

Packages

36800-979-10 — 1 BOTTLE, PLASTIC in 1 CARTON (36800-979-10) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

36800-793 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 36800-900 — Acetaminophen, 36800-905 — Acetaminophen, 36800-914 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 36800-921 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 36800-924 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 36800-925 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 36800-934 — Acetaminophen, Aspirin, Caffeine, 36800-946 — Acetaminophen, 36800-973 — acetaminophen, 36800-991 — Acetaminophen, 37000-517 — Acetaminophen, Phenylephine HCl, Dextromethorphan Hydrobromide, and Guaifenesin, 37000-518 — Acetaminophen, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, and Doxylamine Succinate, 37000-523 — Acetaminophen, Phenylephrine Hydrochloride, Doxylamine Succinate, and Dextromethorphan Hydrobromide, 37000-524 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 37000-598 — Diphenhydramine HCl, Acetaminophen, 37000-810 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 37000-812 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, and Phenylephrine Hydrochloride, 37000-815 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, and phenylephrine hydrochloride, 37000-950 — Acetaminophen, Phenylephrine HCl, +3500 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels