PROVENCE AIR SKIN FIT PACT 02 NATURAL BEIGE

Manufacturer
NATURE REPUBLIC CO., LTD. | Kolmar Korea Co.,LTD. Gwanjeong Factory
Effective date
2021-12-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:22:31

Label at a glance#

ProductPROVENCE AIR SKIN FIT PACT 02 NATURAL BEIGE
Active ingredientZINC OXIDE, OCTINOXATE, OCTISALATE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

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

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

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

DESCRIPTION SECTION

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-439-022021-12-16C16284748780-1ba0f9c33-418b-a910-e053-dadaa90a0b85bd40c02d-aa11-45cd-8461-258858705e06
51346-439-022021-01-29C16284748780-1ba0f9c33-418b-a910-e053-dadaa90a0b85bd40c02d-aa11-45cd-8461-258858705e06

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-43951346-439-01, 51346-439-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ec28aaf7-b862-4bd3-9abc-fb820de1a941bd40c02d-aa11-45cd-8461-258858705e062022-10-21WarningsExact identifier
spl set id: bd40c02d-aa11-45cd-8461-258858705e06

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.