NDC 71609-0009

PREMIUM ULTRA UV PURE SUN

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

PREMIUM ULTRA UV PURE SUN is a Topical Stick in the Human Otc Drug category. It is labeled and distributed by Purecell Korea Co., Ltd.. The primary component is Octinoxate; Diethylamino Hydroxybenzoyl Hexyl Benzoate; Octisalate; Bemotrizinol; Octocrylene.

Product ID71609-0009_56375b26-8b45-74c8-e054-00144ff88e88
NDC71609-0009
Product TypeHuman Otc Drug
Proprietary NamePREMIUM ULTRA UV PURE SUN
Generic NameOctocrylene, Ethylhexyl Methoxycinnamate, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Ethylhexyl Salicylate, Bis-ethylhexyloxyphenol Methoxyphenyl Triazine
Dosage FormStick
Route of AdministrationTOPICAL
Marketing Start Date2017-06-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart352
Labeler NamePurecell Korea Co., Ltd.
Substance NameOCTINOXATE; DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE; OCTISALATE; BEMOTRIZINOL; OCTOCRYLENE
Active Ingredient Strength7 g/100g; g/100g; g/100g; g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71609-0009-1

15 g in 1 CONTAINER (71609-0009-1)
Marketing Start Date2017-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71609-0009-1 [71609000901]

PREMIUM ULTRA UV PURE SUN STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-06-01

Drug Details

Active Ingredients

IngredientStrength
OCTINOXATE7 g/100g

OpenFDA Data

SPL SET ID:56379c3c-8622-0508-e054-00144ff8d46c
Manufacturer
UNII

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