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Target Cough plus Chest Congestion DM Max

NDC 11673-775 · TARGET CORPORATION

Generic nameDextromethorphan HBr, Guaifenesin
Dosage formSOLUTION
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Strength20; 400 mg/20mL; mg/20mL
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

11673-775-08 — 1 BOTTLE in 1 CARTON (11673-775-08) / 237 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11673-421 — guaifenesin, 11673-539 — Guaifenesin, 11673-627 — Dextromethorphan HBr, Guaifenesin, 11673-698 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 11673-716 — dextromethorphan hydrobromide, guaifenesin, 11673-731 — Guaifenesin, 11673-732 — Guaifenesin, 11673-738 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 11673-765 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine HCl, 11673-773 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11673-828 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 11673-840 — Guaifenesin, 11673-843 — Acetaminophen, Dextromethrophan HBr, Phenylephrine HCl, 11673-961 — acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl, 11673-972 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, 11673-975 — DAYTIME COLD AND FLU MULTI SYMPTOM, 11673-976 — NIGHTIME COLD AND FLU, 11673-978 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11673-983 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL, 11822-0046 — Guaifenesin and Pseudoephedrine 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.