CALIFORNIA ALOE FRESH POW DERY SUN- homosalate, octocrylene, ethylhexyl salicylate, butyl methoxydibenzoylmethane stick

CALIFORNIA ALOE FRESH POW DERY SUN by

Drug Labeling and Warnings

CALIFORNIA ALOE FRESH POW DERY SUN by is a Otc medication manufactured, distributed, or labeled by NATURE REPUBLIC CO., LTD., Kolmar Korea Co.,LTD. Gwanjeong Factory. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

HOMOSALATE 9.0%
OCTOCRYLENE 9.0%
ETHYLHEXYL SALICYLATE 4.5%
BUTYL METHOXYDIBENZOYLMETHANE 2.9%

Purpose

Sunscreen

Uses

Protects skin from direct sunlight and UV rays.

WARNINGS

For external use only. Avoid contact with eyes. In the event of contact with eyes, rinse thoroughly with water. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children. Replace cap after use.

Keep out of reach of children.

Directions

Apply adequate amount of the product and thoroughly apply on the areas exposed to the UV rays. Apply the sunscreen product before exposure. Re-apply frequently to maintain protection, especially after perspiring, swimming or toweling.

Inactive Ingredients

POLYETHYLENE, PROPYLHEPTYL CAPRYLATE, DIMETHICONE, SILICA, ISOPROPYL PALMITATE, METHYL METHACRYLATE CROSSPOLYMER, POLYMETHYLSILSESQUIOXANE, DICAPRYLYL CARBONATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, ACRYLATES COPOLYMER, OZOKERITE, FRAGRANCE, LAURYL PEG-8 DIMETHICONE, DEHYDROACETIC ACID, POLYGLYCERYL-2 TRIISOSTEARATE, TOCOPHEROL, YELLOW 5 LAKE(CI 19140), WATER, SEA WATER, BUTYLENE GLYCOL, PHENOXYETHANOL, ALOE BARBADENSIS LEAF EXTRACT, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, MORINDA CITRIFOLIA EXTRACT, PENTYLENE GLYCOL, 1,2-HEXANEDIOL, CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CALIFORNIA ALOE FRESH POW DERY SUN 
homosalate, octocrylene, ethylhexyl salicylate, butyl methoxydibenzoylmethane stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-532
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	1.89 g  in 21 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	1.89 g  in 21 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.94 g  in 21 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.6 g  in 21 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-532-01	21 g in 1 CARTON; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	08/01/2020

Labeler - NATURE REPUBLIC CO., LTD. (631172020)

Registrant - NATURE REPUBLIC CO., LTD. (631172020)

Establishment
Name	Address	ID/FEI	Business Operations
Kolmar Korea Co.,Ltd. Bucheon Factory		963271763	manufacture(51346-532)