PROVENCE AIR SKIN FIT PACT 02 NATURAL BEIGE- zinc oxide, octinoxate, octisalate powder 
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.

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ACTIVE INGREDIENT

Active ingredients: ZINC OXIDE 4.80%, ETHYLHEXYL METHOXYCINNAMATE 3.75%, ETHYLHEXYL SALICYLATE 2.50%

INACTIVE INGREDIENT

Inactive ingredients:

Talc, Triethoxycaprylylsilane, Dimethicone, Boron Nitride, Polymethyl Methacrylate, Silica, Zinc Oxide, Methicone, Synthetic Fluorphlogopite, Triethoxycaprylylsilane, Acrylates/Tridecyl Acrylate/Triethoxysilylpropyl Methacrylate/Dimethicone Methacrylate Copolymer, Ethylhexyl Methoxycinnamate, Nylon-12, Ethylhexyl Salicylate, Magnesium Myristate, Dimethicone, Phenyl Trimethicone, Iron Oxides (CI 77492), Mica, Methicone, 1,2-Hexanediol, Iron Oxides (CI 77491), Mica, Methicone, Glyceryl Caprylate, Iron Oxides (CI 77499), Mica, Methicone, Fragrance, Aloe Barbadensis Leaf Extract, Water, Butylene Glycol, 1,2-Hexanediol, Chamomilla Recutita (Matricaria) Flower Water, Camellia Sinensis Leaf Extract, Butylene Glycol, Water, Lippia Citriodora Leaf Extract, Citric Acid, Sodium Benzoate, Water, Calendula Officinalis Flower Extract, Sodium Benzoate, Citric Acid, Water, Butylene Glycol, Rosa Hybrid Flower Extract, 1,2-Hexanediol, Ethyl Hexanediol, Lavandula Angustifolia (Lavender) Flower Water, Phenoxyethanol

PURPOSE

Purpose: Sunscreen

WARNINGS

Warnings:

For external use only.

Avoid contact with eyes.

Discontinue use if signs of irritation or rashes appear.

Replace the cap after use.

Keep out of reach of children.

DESCRIPTION

Indications & Usage:

The powder pact brightens skin complexion for long lasting hours with its lightweight texture.

Directions:

Apply an appropriate amount to the face evenly.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

PROVENCE AIR SKIN FIT PACT 02 NATURAL BEIGE 
zinc oxide, octinoxate, octisalate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51346-439
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION0.48 g  in 10 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE0.37 g  in 10 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE0.25 g  in 10 g
Inactive Ingredients
Ingredient NameStrength
TALC (UNII: 7SEV7J4R1U)  
Dimethicone (UNII: 92RU3N3Y1O)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51346-439-021 in 1 CARTON12/20/201612/01/2021
1NDC:51346-439-0110 g in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35212/20/201612/01/2021
Labeler - NATURE REPUBLIC CO., LTD. (631172020)
Registrant - NATURE REPUBLIC CO., LTD. (631172020)
Establishment
NameAddressID/FEIBusiness Operations
Kolmar Korea Co.,LTD. Gwanjeong Factory689512611manufacture(51346-439)

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