LBEL

Product NDC

13537-027

11-digit product format

135370027

Labeler code

13537

Product ID

13537-027_dd5be4e2-fa42-4add-bdb3-a7e27bdf2eb1

Type

HUMAN OTC DRUG

Nonproprietary name

Ensulizole, Octinoxate, Octisalate, Oxybenzone, and Titanium dioxide

Dosage form

LOTION

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

ENSULIZOLE; OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE

Active strength

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record