daytime cold flu

Product NDC

79481-5100

11-digit product format

794815100

Labeler code

79481

Product ID

79481-5100_b7f7607a-8b02-4e6f-9aed-651ee8801b40

Type

HUMAN OTC DRUG

Nonproprietary name

acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride

Dosage form

SOLUTION

Route

ORAL

Labeler

Meijer, Inc.

Application

M012

Marketing category

OTC MONOGRAPH DRUG

Marketing start

2023-06-30

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