Village11Factory Waterproof Cica Sun

Manufacturer
PFD Co.,Ltd. | COSON Co., Ltd._Osan Plant
Effective date
2020-12-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:26

Label at a glance#

ProductVillage11Factory Waterproof Cica Sun
Active ingredientOctinoxate, Homosalate, Octisalate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate 6.0%
Homosalate 5.0%
Ethylhexyl Salicylate 4.0%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Propanediol, Salvia Hispanica Seed Extract, Centella Asiatica Extract, Houttuynia Cordata Extract, Propanediol, 1,2-Hexanediol, Dimethicone Crosspolymer, Fructooligosaccharides, Saccharide Hydrolysate, Pullulan, Pentylene Glycol, Phenoxyethanol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Fragrance, Triethanolamine, Ethylhexylglycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Octyldodecanol, Echium Plantagineum Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Cardiospermum Halicacabum Flower/Leaf/Vine Extract, Tocopherol, Anthemis Nobilis Flower Extract, Butylene Glycol, Aloe Barbadensis Leaf Extract, Calendula Officinalis Flower Extract, Persea Gratissima (Avocado) Fruit Extract, Xanthan Gum, Glyceryl Stearate, PEG-100 Stearate, Polyglyceryl-3 Methylglucose Distearate, Polysorbate 20, Polyacrylate Crosspolymer-6, t-Butyl Alcohol, C12-15 Alkyl Benzoate, Titanium Dioxide (CI 77891), Aluminum Stearate, Polyhydroxystearic Acid, Alumina, Oleth-10, Isodeceth-6, Simethicone, Dimethicone

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

WARNINGS

WARNINGS SECTION

For external use only
Avoid contact with eyes.
Discontinue use if signs of irritation or rashes appear.
Do not apply on broken skin or wounded areas.
Keep out of reach of children
Store away from direct sunlight.

DESCRIPTION

DESCRIPTION SECTION

Uses:

■ Helps prevent sun burn. Waterproof Sun Lotion that moisturizes the skin and prevents sun burn even when in contact with sweat, water, and sebum.

Directions:

■ Apply liberally and uniformly to all exposed areas 15-20 minutes before sun exposure.
■ Reapply often (every 2 hours) and after swimming, excessive perspiration and washing to ensure maximum sun protection.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72470-040-022022-01-28C16284748780-1d6a99b39-b498-a426-e053-dadaa90af4c2581bf100-43b8-4180-bd25-6afebe35761e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72470-040-01Village11Factory Waterproof Cica Sun80 mL in 1 CONTAINERLOTION801
72470-040-02Village11Factory Waterproof Cica Sun1 in 1 CARTONLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72470-040VILLAGE11FACTORY WATERPROOF CICA SUN (OCTINOXATE, HOMOSALATE, OCTISALATE) LOTION [PFD CO.,LTD.]1Legacy NDC, 2 package rows20201202_581bf100-43b8-4180-bd25-6afebe35761e.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72470-04072470-040-01, 72470-040-02

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
9160c756-6f64-4849-ad36-4334b0f03c83581bf100-43b8-4180-bd25-6afebe35761e2020-12-01WarningsExact identifier
spl id: 9160c756-6f64-4849-ad36-4334b0f03c83
spl set id: 581bf100-43b8-4180-bd25-6afebe35761e

Reported adverse events (FAERS/openFDA)#

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