Daytime

Product NDC

68016-199

11-digit product format

680160199

Labeler code

68016

Product ID

68016-199_bc71e159-c968-4ce6-b15c-35be7cef6552

Type

HUMAN OTC DRUG

Nonproprietary name

Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Chain Drug Consortium, LLC

Application

part341

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2012-11-15

Marketing end

0000-00-00

Substance

ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE

Active strength

325 mg/1; mg/1; mg/1

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record