FDA.reportPublic FDA data

LIGHT CARE AQUA SUN

Manufacturer
WOW VENTURES | Cosmecca Korea Co.,Ltd.
Effective date
2015-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:42:50

Label at a glance#

ProductLIGHT CARE AQUA SUN
Active ingredientOctinoxate, Octocrylene, Octisalate, Avobenzone
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Ethylhexyl Methoxycinnamate 7.0%, Octocrylene 5.0%, Ethylhexyl Salicylate 4.5%, Butyl Methoxydibenzoylmethane 4.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Chamaecyparis Obtusa Water, Butylene Glycol, Alcohol Denat., Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Methyl Methacrylate Crosspolymer, Dipropylene Glycol, Polysorbate 60, Dimethicone, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylyl Glycol, Cyclopentasiloxane, Methoxy PEG/PPG-25/4 Dimethicone, Bis-PEG/PPG-20/5 PEG/PPG-20/5 Dimethicone, Isohexadecane, Phenoxyethanol, Ethylhexylglycerin, Fragrance, Polysorbate 80, Cyclohexasiloxane, Caprylic/Capric Triglyceride, 1,2-Hexanediol, BHT, Potassium Hydroxide, Disodium EDTA, Water, Rosa Canina Fruit Oil, Sea Water, Melaleuca Alternifolia (Tea Tree) Leaf Water, Propylene Glycol, Aspalathus Linearis Leaf Extract, Hamamelis Virginiana (Witch Hazel) Water, Caulerpa Lentillifera Extract, Glycerin, Alcohol, Pentylene Glycol, Hippophae Rhamnoides Fruit Extract, Camellia Sinensis Leaf Extract, Sodium Hyaluronate, Hydrolyzed Collagen

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: 1. If any of the following symptoms appear on the area where the product was applied, stop using the product immediately and consult a specialist. A. Redness, swelling, itchiness, irritation or other abnormal symptoms B. Symptoms above appear after exposure to direct sunlight 2. DO NOT use the product on an area with wound, eczema, or dermatitis 3. Storage and handling. A. Make sure to close the lid after use B. Keep away from children and babies C. DO NOT store in a place with high or low temperature and direct sunlight 4. Use the product once a week due to high content of Vitamin C. If your skin is not irritated or sensitive either, you can apply it twice or three times a week.

DESCRIPTION

DESCRIPTION SECTION

Directions & Usage: Apply a suitable amount to and spread evenly on your skin that would be exposed to sun after all basic skin care.

Dosage & Administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69894-100-012020-01-31C16284748780-19d75b9d0-9f3d-f424-e053-dadaa90a57ceae28ea61-b1f4-451c-b439-551f05bda0a7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69894-100-01LIGHT CARE AQUA SUN50 mL in 1 CARTONGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69894-100LIGHT CARE AQUA SUN (OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE) GEL [WOW VENTURES]1Legacy NDC, 1 package rows20150624_ae28ea61-b1f4-451c-b439-551f05bda0a7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AvobenzoneACTIVE INGREDIENTG63QQF2NOX1
OctinoxateACTIVE INGREDIENT4Y5P7MUD511
OctisalateACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM1
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA1

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
69894-10069894-100-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
Octinoxate4Y5P7MUD51ACTIB
Octocrylene5A68WGF6WMACTIB
Octisalate4X49Y0596WACTIB
AvobenzoneG63QQF2NOXACTIB
Butylene Glycol3XUS85K0RAIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
32495787-4fc4-40e9-8729-ff4c52eeafceae28ea61-b1f4-451c-b439-551f05bda0a72015-06-24WarningsExact identifier
spl id: 32495787-4fc4-40e9-8729-ff4c52eeafce
spl set id: ae28ea61-b1f4-451c-b439-551f05bda0a7

Reported adverse events (FAERS/openFDA)#

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