Anti Bacterial Foam Hand Problend

Product NDC

76250-995

11-digit product format

762500995

Labeler code

76250

Product ID

76250-995_4581e04a-bd9e-4989-bce1-3b8cf1d0b420

Type

HUMAN OTC DRUG

Nonproprietary name

benzalkonium chloride

Dosage form

SOAP

Route

TOPICAL

Labeler

Seatex Ltd

Application

part333E

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2012-05-31

Marketing end

0000-00-00

Substance

BENZALKONIUM CHLORIDE

Active strength

1 g/1000mL

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record