Maximum Strength Cold Flu and Sore Throat

NDC 30142-731 · KROGER COMPANY

Generic nameAcetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl

Dosage formSOLUTION

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

30142-731-06 — 180 mL in 1 BOTTLE, PLASTIC (30142-731-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

30142-561 — Acetaminophen, 30142-586 — Acetaminophen, Aspirin, Caffeine, 30142-590 — acetaminophen, 30142-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 30142-625 — Acetaminophen, Aspirin, Caffeine, 30142-698 — Acetaminophen, Chlorpheniramine maleate, 30142-713 — Glycerin, Lidocaine, Petrolatum, Phenylephrine HCl, 30142-720 — Acetaminophen, Ibuprofen, 30142-722 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, GUAIFENESIN PHENYLEPHRINE HCL, 30142-727 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 30142-732 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 30142-736 — Acetaminophen , Diphenhydramine HCl,Phenylephrine HCl, 30142-738 — Dextromethorphan HBr, Guaifenesin, and Phenylephrine HCl, 30142-739 — guaifenesin and pseudoephedrine hydrochloride, 30142-755 — Acetaminophen and Diphenhydramine Hydrochloride, 30142-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 30142-766 — Acetaminophen, 30142-780 — brompheniramine maleate, dextromethorphan hydrobromide, 30142-818 — Acetaminophen, 30142-828 — Acetaminophen, Guaifenesin, 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels