QUALITY CHOICE Maximum Strength Daytime Cold and Flu

Product NDC

83324-162

11-digit product format

833240162

Labeler code

83324

Product ID

83324-162_2e1a6543-5b2c-450b-9cc1-b4e5efb89f96

Type

HUMAN OTC DRUG

Nonproprietary name

Acetaminophen, Dextromethorphan hydrobromide, Guaifenesin, Phenylephrine hydrochloride

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Chain Drug Marketing Association, Inc.

Application

M012

Marketing category

OTC MONOGRAPH DRUG

Marketing start

2025-11-04

Substance

ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE

Active strength

325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1

Pharmacologic classes

Adrenergic 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]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes