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Product NDC

82442-119

11-digit product format

824420119

Labeler code

82442

Product ID

82442-119_89f6918b-b13c-4cca-9844-bf536e525ef4

Type

HUMAN OTC DRUG

Nonproprietary name

acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride

Dosage form

SOLUTION

Route

ORAL

Labeler

Target Corporation

Application

M012

Marketing category

OTC MONOGRAPH DRUG

Marketing start

2024-06-06

Substance

ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE

Active strength

325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL

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