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CVS Maximum Strength Cold and Flu Relief

NDC 69842-566 · CVS PHARMACY, INC

Generic nameAcetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased 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], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

69842-566-06 — 180 mL in 1 BOTTLE, PLASTIC (69842-566-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-450 — Acetaminophen, 69842-465 — Acetaminophen, 69842-475 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-484 — Acetaminophen, 69842-487 — Childrens Stuffy Nose and Cold, 69842-491 — Acetaminophen, 69842-503 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-505 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-513 — dextromethorphan hydrobromide, guaifenesin, 69842-541 — Acetaminophen, Aspirin, Caffeine, 69842-570 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-572 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, 69842-577 — DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN, 69842-586 — Acetaminophen, Aspirin, Caffeine, 69842-591 — Acetaminophen 250mg Aspirin 250mg Caffeine 65mg, 69842-592 — Acetaminophen 250mg Aspirin 250mg Caffeine 65mg, 69842-616 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 69842-634 — Dextromethorphan HBr, 69842-635 — Acetaminophen, 69842-639 — Brompheniramine maleate, Phenylephrine HCl, +5267 more

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