ESIKA

Product NDC

13537-310

11-digit product format

135370310

Labeler code

13537

Product ID

13537-310_fdc926fe-0aac-44f6-b687-b4980f5027f4

Type

HUMAN OTC DRUG

Nonproprietary name

Octinoxate and Oxybenzone

Dosage form

LOTION

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; OXYBENZONE

Active strength

0 mg/mL; mg/mL

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record