UV Defense Pocket Sun Pad (Broad Spectrum, SPF30)

Product NDC

71621-0011

11-digit product format

716210011

Labeler code

71621

Product ID

71621-0011_685648ae-d715-0a4b-e053-2a91aa0acf9a

Type

HUMAN OTC DRUG

Nonproprietary name

octocrylene

Dosage form

LIQUID

Route

TOPICAL

Labeler

C&TECH CORPORATION

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2018-03-01

Marketing end

0000-00-00

Substance

OCTOCRYLENE; HOMOSALATE; OCTISALATE; AVOBENZONE

Active strength

10 g/100g; g/100g; g/100g; g/100g

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record