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Product NDC

13537-109

11-digit product format

135370109

Labeler code

13537

Product ID

13537-109_3bd7c666-3e6f-4828-9ea7-c2bdc9b2fdbe

Type

HUMAN OTC DRUG

Nonproprietary name

Octinoxate and Oxybenzone

Dosage form

LIPSTICK

Route

TOPICAL

Labeler

Ventura Corporation LTD

Application

part352

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2014-01-31

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