Celox Ultra

Product NDC

75990-007

11-digit product format

759900007

Labeler code

75990

Product ID

75990-007_87ae6fae-62b6-42f3-9e18-394f2c039677

Type

HUMAN OTC DRUG

Nonproprietary name

ALCOHOL

Dosage form

LIQUID

Route

TOPICAL

Labeler

Certus Medical, Inc.

Application

part333E

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2011-04-25

Marketing end

0000-00-00

Substance

ALCOHOL

Active strength

1 mL/mL

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record