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Product NDC

13537-195

11-digit product format

135370195

Labeler code

13537

Product ID

13537-195_70dd741b-bce1-4075-b3a7-03d4c61999af

Type

HUMAN OTC DRUG

Nonproprietary name

Octinoxate, Oxybenzone, and Titanium Dioxide

Dosage form

CREAM

Route

TOPICAL

Labeler

Ventura Corporation LTD

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2014-03-06

Marketing end

0000-00-00

Substance

OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE

Active strength

0 g/g; g/g; g/g

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record