CALIFORNIA ALOE FRESH POW DERY SUN- octocrylene, octinoxate, octisalate 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.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: OCTOCRYLENE 9.00%, ETHYLHEXYL METHOXYCINNAMATE 7.00%, ETHYLHEXYL SALICYLATE 4.50%

INACTIVE INGREDIENT

Inactive ingredients:
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, POLYETHYLENE, DIMETHICONE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, METHYL METHACRYLATE CROSSPOLYMER, SILICA, CETYL ETHYLHEXANOATE, DICAPRYLYL CARBONATE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, TOCOPHERYL ACETATE, OZOKERITE, ALOE BARBADENSIS LEAF EXTRACT, MORINDA CITRIFOLIA EXTRACT, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, BISABOLOL, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, DEHYDROACETIC ACID, SEA WATER, WATER, BUTYLENE GLYCOL, FRAGRANCE, PHENOXYETHANOL

PURPOSE

Purpose: Sunscreen

WARNINGS

Warnings:
For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children. Replace the cap after use.

DESCRIPTION

Uses:
Brightening, Wrinkle-improvement, UV Protection.
A moisture-rich daily sun block that purifies and corrects your skin tone.

Directions: 

Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays..

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CALIFORNIA ALOE FRESH POW DERY SUN 
octocrylene, octinoxate, octisalate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-517
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	1.98 g  in 22 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.54 g  in 22 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.99 g  in 22 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-517-02	1 in 1 CARTON	12/01/2018
1	NDC: 51346-517-01	22 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	12/01/2018

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

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

Establishment
Name	Address	ID/FEI	Business Operations
Kolmar Korea Co., Ltd.		689512611	manufacture(51346-517)