Pure Hands

Product NDC

50539-221

11-digit product format

505390221

Labeler code

50539

Product ID

50539-221_32cc712f-dc81-4e98-945b-c57f47c9d77c

Type

HUMAN OTC DRUG

Nonproprietary name

ALCOHOL

Dosage form

GEL

Route

TOPICAL

Labeler

Buck Head Products & Systems

Application

part333

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2009-12-01

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