ESIKA

Product NDC

13537-320

11-digit product format

135370320

Labeler code

13537

Product ID

13537-320_d6c64fef-cbe6-4ccd-92d4-803463c61be2

Type

HUMAN OTC DRUG

Nonproprietary name

OCTINOXATE

Dosage form

POWDER

Route

TOPICAL

Labeler

Ventura Corporation (San Juan, P.R)

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2011-05-17

Marketing end

0000-00-00

Substance

OCTINOXATE

Active strength

0 g/g

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record