DayQuil Severe

Product NDC

66715-9704

11-digit product format

667159704

Labeler code

66715

Product ID

66715-9704_ee00b795-94b6-278b-e053-2a95a90a7b9d

Type

HUMAN OTC DRUG

Nonproprietary name

Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Lil' Drug Store Products, Inc

Application

part341

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2013-06-21

Marketing end

0000-00-00

Substance

ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE

Active strength

325 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

2023-12-31

Current FDA listing

Historical FDA.report record