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Headache Relief

NDC 49035-433 · Wal-Mart Stores Inc

Generic nameAcetaminophen, Aspirin and Caffeine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, ASPIRIN, CAFFEINE
Strength250; 250; 65 mg/1; mg/1; mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
Marketing categoryOTC MONOGRAPH DRUG

Packages

49035-433-06 — 2 BOTTLE, PLASTIC in 1 CARTON (49035-433-06) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49035-433-12)

49035-433-08 — 1 BOTTLE, PLASTIC in 1 CARTON (49035-433-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49035-193 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 49035-226 — Caffeine, 49035-274 — Aspirin, 49035-278 — Acetaminophen, 49035-308 — Acetaminophen, 49035-313 — Acetaminophen, 49035-324 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 49035-336 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 49035-363 — Acetaminophen, Diphenhydramine HCl, 49035-421 — Aspirin, Citric Acid, Sodium Bicarbonate, 49035-455 — Acetaminophen, 49035-466 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 49035-467 — Aspirin, 49035-476 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 49035-478 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 49035-527 — Acetaminophen, Guaifenesin and Phenylephrine HCl, 49035-531 — Acetaminophen, 49035-543 — Acetaminophen, Diphenhydramine HCl, Phenylephrine HCl, 49035-563 — Aspirin, 49035-609 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, +4118 more

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