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equate pain relief

NDC 79903-422 · WALMART INC.

Generic nameacetaminophen
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETAMINOPHEN
Strength1000 mg/30mL
Marketing categoryOTC MONOGRAPH DRUG

Packages

79903-422-12 — 355 mL in 1 BOTTLE (79903-422-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

79903-355 — acetaminophen, dextromethorphan hydrobromide, 79903-356 — acetaminophen, diphenhydramine hydrochloride, 79903-370 — Acetaminophen, Aspirin, Caffeine, 79903-373 — acetaminophen,caffeine, 79903-386 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 79903-387 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine Hydrochloride, 79903-416 — acetaminophen, dextromethorphan hydrobromide, 79903-418 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 79903-420 — acetaminophen, 79903-421 — acetaminophen, diphenhydramine hydrochloride, 79903-433 — Acetaminophen, Dextromethorphan HBr, 79903-434 — Acetaminophen, Diphenhydramine HCl, 79903-931 — Acetaminophen and Ibuprofen (NSAID), 80272-002 — Acetaminophen, 80425-0215 — Butalbital/Acetaminophen/Caffeine, 80425-0497 — butalbital, acetaminophen and caffeine, 80425-0527 — Acetaminophen and Codeine Phosphate, 80425-0528 — Acetaminophen and Codeine Phosphate, 80425-0529 — Acetaminophen and Codeine Phosphate, 80425-0530 — Acetaminophen and Codeine Phosphate, +3476 more

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