CALIFORNIA ALOE DAILY SUN BLOCK- zinc oxide, homosalate, ethylhexyl salicylate, titanium dioxide cream 
NATURE REPUBLIC CO., LTD.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

ACTIVE INGREDIENTS

ZINC OXIDE 12.7%
HOMOSALATE 7.5%
ETHYLHEXYL SALICYLATE 4.5%
TITANIUM DIOXIDE 2.2%

INACTIVE INGREDIENTS

WATER, CYCLOPENTASILOXANE, COCO-CAPRYLATE/CAPRATE, DIPROPYLENE GLYCOL, LAURYL PEG-10 TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE, GLYCERIN, NIACINAMIDE, BUTYLOCTYL SALICYLATE, METHYL METHACRYLATE CROSSPOLYMER, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, DIMETHICONE, 1,2-HEXANEDIOL, TRIETHOXYCAPRYLYLSILANE, STEARIC ACID, ALUMINUM HYDROXIDE, SORBITAN CAPRYLATE, DIMETHICONE/PEG-10/15 CROSSPOLYMER, FRAGRANCE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, DICAPRYLYL CARBONATE, GLYCERYL CAPRYLATE, MICA, IRON OXIDES(CI 77492), ETHYLHEXYLGLYCERIN, ADENOSINE, IRON OXIDES(CI 77491), SODIUM CITRATE, IRON OXIDES(CI 77499), SEA WATER, BUTYLENE GLYCOL, TOCOPHEROL, ALOE BARBADENSIS LEAF EXTRACT, PHENOXYETHANOL, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, MORINDA CITRIFOLIA EXTRACT, PENTYLENE GLYCOL, CAPRYLYL GLYCOL

PURPOSE

Sunscreen

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.

DESCRIPTION

Uses
Protects skin from direct sunlight and UV rays.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

CALIFORNIA ALOE DAILY SUN BLOCK 
zinc oxide, homosalate, ethylhexyl salicylate, titanium dioxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51346-533
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION7.23 g  in 57 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE4.27 g  in 57 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE2.56 g  in 57 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE1.25 g  in 57 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51346-533-0157 mL in 1 CARTON; Type 0: Not a Combination Product08/01/202012/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35208/01/202012/01/2021
Labeler - NATURE REPUBLIC CO., LTD. (631172020)
Registrant - NATURE REPUBLIC CO., LTD. (631172020)
Establishment
NameAddressID/FEIBusiness Operations
Kolmar Korea Co.,LTD. Gwanjeong Factory689512611manufacture(51346-533)

Revised: 10/2022
 
NATURE REPUBLIC CO., LTD.