LBEL COULEUR LUXE AMPLIFIER XP

Product NDC

13537-548

11-digit product format

135370548

Labeler code

13537

Product ID

13537-548_bda95f66-6663-44ca-9320-bc31d6e01a7d

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

2013-05-27

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