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Cold and Flu

NDC 49035-193 · EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)

Generic nameAcetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 5 mg/1; mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

49035-193-24 — 24 BLISTER PACK in 1 CARTON (49035-193-24) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

49035-193-48 — 48 BLISTER PACK in 1 CARTON (49035-193-48) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

47781-230 — Oxycodone and Acetaminophen, 48201-001 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 49035-042 — Acetaminophen, 49035-044 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 49035-053 — Acetaminophen,Dextromethorphan HBr,Guaifenesin,Phenylephrine HCl, 49035-082 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 49035-165 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 49035-175 — Acetaminophen, 49035-181 — Acetaminophen, 49035-188 — mineral oil, petrolatum, phenylephrine HCl, 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, 49035-384 — dextromethorphan polistirex, 49035-433 — Acetaminophen, Aspirin and Caffeine, 49035-455 — Acetaminophen, 49035-463 — cocoa butter, phenylephrine HCl, +4867 more

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