EFFET PARFAIT HYDRATESS

Product NDC

13537-911

11-digit product format

135370911

Labeler code

13537

Product ID

13537-911_1a5fda67-78a1-436c-bf44-42c32031e809

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

2014-09-12

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