LBEL

Product NDC

13537-019

11-digit product format

135370019

Labeler code

13537

Product ID

13537-019_0b153b98-72fc-4125-b437-d0fa7fc058c2

Type

HUMAN OTC DRUG

Nonproprietary name

OCTINOXATE and OXYBENZONE

Dosage form

LIPSTICK

Route

TOPICAL

Labeler

Ventura Corporation Ltd.

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2011-08-10

Marketing end

0000-00-00

Substance

OCTINOXATE; OXYBENZONE

Active strength

0 g/g; g/g

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record