Derma Brilliance Sunscreen SPF 30

Product NDC

62742-4073

11-digit product format

627424073

Labeler code

62742

Product ID

62742-4073_2cf57334-fa04-41f3-964d-edbe1dc8f31e

Type

HUMAN OTC DRUG

Nonproprietary name

Octinoxate, Oxybenzone, Octisalate, Avobenzone and Octocrylene

Dosage form

CREAM

Route

TOPICAL

Labeler

Allure Labs, Inc

Application

part352

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2015-03-17

Marketing end

0000-00-00

Substance

OCTINOXATE; OXYBENZONE; OCTISALATE; AVOBENZONE; OCTOCRYLENE

Active strength

8 mg/g; mg/g; mg/g; mg/g; mg/g

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record