PREMIUM ULTRA UV PURE SUN

Product NDC

71609-0009

11-digit product format

716090009

Labeler code

71609

Product ID

71609-0009_56375b26-8b45-74c8-e054-00144ff88e88

Type

HUMAN OTC DRUG

Nonproprietary name

Octocrylene, Ethylhexyl Methoxycinnamate, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Ethylhexyl Salicylate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine

Dosage form

STICK

Route

TOPICAL

Labeler

Purecell Korea Co., Ltd.

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2017-06-01

Marketing end

0000-00-00

Substance

OCTINOXATE; DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE; OCTISALATE; BEMOTRIZINOL; OCTOCRYLENE

Active strength

7 g/100g; g/100g; g/100g; g/100g; g/100g

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record