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Mucinex Fast-Max Cold, Flu and Sore Throat

NDC 72854-162 · Reckitt Benckiser LLC

Generic nameAcetaminophen, Guaifenesin
Dosage formTABLET
RouteORAL
Active ingredient(s)ACETAMINOPHEN, GUAIFENESIN
Strength325; 200 mg/1; mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

72854-162-20 — 2 BLISTER PACK in 1 CARTON (72854-162-20) / 10 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72854-128 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 72854-136 — Acetaminophen, Guaifenesin, 72854-137 — Dextromethorphan HBr, Guaifenesin, 72854-138 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 72854-140 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, and TRIPROLIDINE HYDROCHLORIDE, 72854-143 — Acetaminophen, Dextromethorphan Hydrobromide, Triprolidine Hydrochloride, 72854-153 — Dextromethorphan Hydrobromide, Guaifenesin, 72854-157 — Dextromethorphan hydrobromide, Guaifenesin, 72854-159 — Dextromethorphan Hydrobromide, Guaifenesin, 72854-161 — Acetaminophen, Dextromethorphan Hydrobromide, 72854-163 — acetaminophen, dextromethorphan hydrobromide, and triprolidine hydrochloride, 72854-164 — Acetaminophen, Guaifenesin, 72854-167 — Acetaminophen, Dextromethorphan Hydrobromide, Triprolidine Hydrochloride, 72854-171 — Acetaminophen, Dextromethorphan Hydrobromide, 72854-202 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 72854-203 — Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride, 72854-208 — Acetaminophen, Guaifenesin, 72854-209 — Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride, 72854-211 — Acetaminophen and Guaifenesin, 72854-214 — Acetaminophen, Dextromethorphan Hydrobromide, +4498 more

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