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CVS Chest Congestion Relief

NDC 69842-996 · CVS Pharmacy, Inc.

Generic nameDextromethorphan Hydrobromide / Guaifenesin
Dosage formTABLET
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Strength20; 400 mg/1; mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
Marketing categoryOTC MONOGRAPH DRUG

Packages

69842-996-30 — 1 BOTTLE, PLASTIC in 1 CARTON (69842-996-30) / 30 TABLET in 1 BOTTLE, PLASTIC

69842-996-60 — 1 BOTTLE, PLASTIC in 1 CARTON (69842-996-60) / 60 TABLET in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-903 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL, 69842-904 — Dextromethorphan Hydrobromide Guaifenesin, 69842-926 — Dextromethorphan HBr, Guaifenesin, 69842-933 — Guaifenesin, Dextromethorphan HBr, 69842-937 — Dextromethorphan HBr and Guaifenesin, 69842-942 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-947 — Acetaminophen, Dextromethorphan HBr, 69842-963 — guaifenesin, dextromethorphan hydrobromide, 69842-966 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, and TRIPROLIDINE HYDROCHLORIDE, 69842-969 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCL, 69842-997 — Guaifenesin/phenylephrine, 69848-017 — Guaifenesin, 69848-018 — Guaifenesin, 70000-0050 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 70000-0055 — Guaifenesin, 70000-0056 — Dextromethorphan Hydrobromide / Guaifenesin, 70000-0080 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 70000-0083 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 70000-0133 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, 70000-0141 — Guaifenesin, Phenylephrine HCl, +2508 more

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