Pure Gel

Product NDC

50452-221

11-digit product format

504520221

Labeler code

50452

Product ID

50452-221_6587cd4a-676b-4a03-b5ad-14006c19a37c

Type

HUMAN OTC DRUG

Nonproprietary name

ALCOHOL

Dosage form

GEL

Route

TOPICAL

Labeler

Phoenix Research Industries, Inc.

Application

part333

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2010-02-01

Marketing end

0000-00-00

Substance

ALCOHOL

Active strength

1 mL/mL

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record