LBel

Product NDC

13537-230

11-digit product format

135370230

Labeler code

13537

Product ID

13537-230_f1107067-ec96-4c76-9812-fa3ad7d196ce

Type

HUMAN OTC DRUG

Nonproprietary name

Octinoxate

Dosage form

LOTION

Route

TOPICAL

Labeler

VENTURA INTERNATIONAL LTD.,

Application

part352

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2010-08-15

Marketing end

0000-00-00

Substance

OCTINOXATE

Active strength

2 g/30mL

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record