STEBLANC WATER CC PACT

Manufacturer
Coson Co., Ltd.
Effective date
2014-09-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:40:16

Label at a glance#

ProductSTEBLANC WATER CC PACT 23 Natural Beige
Active ingredientTitanium Dioxide, Octinoxate, Octisalate, Octocrylene, Zinc Oxide
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: Titanium Dioxide 9.0055%, Ethylhexyl Methoxycinnamate 7%, Ethylhexyl Salicylate 4.8%, Octocrylene 2%, Zinc Oxide 2%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS:
Water, Cyclopentasiloxane, C12-15 Alkyl benzoate, Cyclohexasiloxane, Glycerin, Niacinamide, PEG-30 Dipolyhydroxystearate, Quaternium-18 Bentonite, PEG-10 Dimethicone, Butylene Glycol, Sodium Chloride, Iron Oxides (CI 77492), Dimethicone, Iron Oxides (CI 77491), Ozokerite, Copernicia Cerifera (Carnauba) Wax, Chlorphenesin, Perfume, Triethoxycaprylylsilane, Aluminum Hydroxide, Iron Oxides (CI 77499),Adenosine, Centella Asiatica Extract, Portulaca Oleracea Extract, Vitex Agnus Castus Extract, Chamomilla Recutita (Matricaria) Flower

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: UVA/UVB Protection

WARNINGS

WARNINGS SECTION

WARNINGS:
1. If following symptoms occur, stop use and consult a doctor: red spots, swelling, itcihng, irritation, or symtoms on applied skin under direct sunlight.
2. Do not use on scarred skin, or if you have dermatitis or eczema
3. Keep the cap close on its product
4. Keep away from direct sunlight or heat.
5. This product blocks UVA rays and ultraviolet protection effectiveness have been measured by the Food and Drug Administration methods and standards

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children: Keep out of reach of babies and children

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

INDICATION & USAGE:
At the step of base make-up, tap the products gentlely on your face with the puff and let it absorb.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION:
At the stage of base make-up, apply it a suitable amount by using the provided applier.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62171-060-012020-01-31C16284748780-19d75b9cf-f029-f424-e053-dadaa90a57ce1e0ffee2-e45d-4bad-b67d-a44c39ede7de

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62171-060-01STEBLANC WATER CC PACT23 Natural Beige13 g in 1 CARTONPOWDER131

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62171-060STEBLANC WATER CC PACT 23 NATURAL BEIGE (TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE) POWDER [COSON CO., LTD.]1Legacy NDC, 1 package rows20140923_1e0ffee2-e45d-4bad-b67d-a44c39ede7de.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OctinoxateACTIVE INGREDIENT4Y5P7MUD511
OctisalateACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
Zinc OxideACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC CATIONACTIVE MOIETY13S1S8SF371
C12-15 Alkyl benzoateINACTIVE INGREDIENTA9EJ3J61HQ1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62171-06062171-060-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
5df2f2af-e89b-4a14-9813-dfb0695753711e0ffee2-e45d-4bad-b67d-a44c39ede7de2014-09-23WarningsExact identifier
spl id: 5df2f2af-e89b-4a14-9813-dfb069575371
spl set id: 1e0ffee2-e45d-4bad-b67d-a44c39ede7de

Reported adverse events (FAERS/openFDA)#

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