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Kroger Chest Congestion Relief

NDC 30142-472 · THE KROGER CO

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

30142-472-30 — 1 BOTTLE in 1 CARTON (30142-472-30) / 30 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

30142-086 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 30142-087 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 30142-137 — Guaifenesin and Pseudoephedrine HCl, 30142-275 — Guaifenesin and Dextromethorphan HBr, 30142-276 — Guaifenesin and Dextromethorphan HBr, 30142-292 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 30142-335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 30142-384 — dextromethorphan polistirex, 30142-470 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 30142-471 — Guaifenesin, 30142-494 — dextromethorphan polistirex, 30142-508 — Dextromethorphan Hydrobromide Guaifenesin, 30142-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 30142-722 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, GUAIFENESIN PHENYLEPHRINE HCL, 30142-727 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 30142-731 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 30142-732 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 30142-738 — Dextromethorphan HBr, Guaifenesin, and Phenylephrine HCl, 30142-739 — guaifenesin and pseudoephedrine hydrochloride, 30142-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 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.