Foaming Hand Sanitizer

Product NDC

0869-0492

11-digit product format

008690492

Labeler code

0869

Product ID

0869-0492_62a8623b-6501-4af9-94d1-9fb3f0b724a6

Type

HUMAN OTC DRUG

Nonproprietary name

Benzalkonium chloride

Dosage form

LIQUID

Route

TOPICAL

Labeler

Vi-Jon

Application

part333A

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2014-09-03

Marketing end

0000-00-00

Substance

BENZALKONIUM CHLORIDE

Active strength

1 mg/mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record