Principal Secret

Product NDC

11410-541

11-digit product format

114100541

Labeler code

11410

Product ID

11410-541_48c30b3c-7c9c-4371-a3b4-1443d9269a4d

Type

HUMAN OTC DRUG

Nonproprietary name

Octinoxate and Octisalate

Dosage form

CREAM

Route

TOPICAL

Labeler

Guthy-Renker LLC

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2002-05-10

Marketing end

0000-00-00

Substance

OCTINOXATE; OCTISALATE

Active strength

8 mg/.1g; mg/.1g

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record