NDC 58832-0001

LUACELL Illuminating White Label Sun Cream

Homosalate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane, Octocrylene

LUACELL Illuminating White Label Sun Cream is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Eyesome. Co.,ltd.. The primary component is Octocrylene; Octisalate; Avobenzone; Homosalate.

Product ID58832-0001_91391db6-1229-660f-e053-2a95a90aec60
NDC58832-0001
Product TypeHuman Otc Drug
Proprietary NameLUACELL Illuminating White Label Sun Cream
Generic NameHomosalate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane, Octocrylene
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2019-08-28
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart352
Labeler NameEYESOME. Co.,Ltd.
Substance NameOCTOCRYLENE; OCTISALATE; AVOBENZONE; HOMOSALATE
Active Ingredient Strength3 g/100mL; g/100mL; g/100mL; g/100mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 58832-0001-1

3 TUBE in 1 CONTAINER (58832-0001-1) > 25 mL in 1 TUBE
Marketing Start Date2019-08-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58832-0001-1 [58832000101]

LUACELL Illuminating White Label Sun Cream CREAM
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-08-28

Drug Details

Active Ingredients

IngredientStrength
OCTOCRYLENE2.5 g/100mL

OpenFDA Data

SPL SET ID:91392b71-79bb-2302-e053-2a95a90a89be
Manufacturer
UNII

NDC Crossover Matching brand name "LUACELL Illuminating White Label Sun Cream" or generic name "Homosalate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane, Octocrylene"

NDCBrand NameGeneric Name
58832-0001LUACELL Illuminating White Label Sun CreamHomosalate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane, Octocrylene
58832-0002XIELL Intensive Cell Recovery Sun CreamHomosalate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane, Octocrylene

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.