W.SKIN TRIPLE CARE SUN

Manufacturer
J&J COMPANY
Effective date
2021-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:40:15

Label at a glance#

ProductW.SKIN TRIPLE CARE SUN
Active ingredientOCTOCRYLENE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Octocrylene

INACTIVE INGREDIENT SECTION

Cetyl Ethylhexanoate, Ethylhexyl Palmitate, Synthetic Wax, Octocrylene, Dimethicone, Ceresin, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate , Methyl Methacrylate Crosspolymer, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Dicaprylyl Carbonate, Butylene Glycol Dicaprylate/Dicaprate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Microcrystalline Wax, Cyclopentasiloxane, Sorbitan Olivate, Dimethicone/Vinyl Dimethicone Crosspolymer, Disteardimonium Hectorite, Centella Asiatica Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Daucus Carota Sativa (Carrot) Root Extract, Citrullus Vulgaris (Watermelon) Fruit Extract, Solanum Lycopersicum (Tomato) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Fragaria Ananassa (Strawberry) Fruit Extract, Prunus Serotina (Wild Cherry) Fruit Extract, Rubus Idaeus (Raspberry) Fruit Extract, Prunus Salicina Fruit Extract, Vaccinium Macrocarpon (Cranberry) Fruit Extract, Punica Granatum Fruit Extract, Citrus Paradisi (Grapefruit) Seed Extract, Capsicum Annuum Fruit Extract, Capsicum Annuum Extract, Psidium Guajava Fruit Extract, Wine Extract, Caprylyl Glycol, Triethyl Citrate, Tocopheryl Acetate, Ethylhexylglycerin, Fragrance, Geraniol, Butylphenyl Methylpropional, Limonene, Linalool

OTC - PURPOSE SECTION

It has a strong sun block and waterproof function. Matt type sun stick that applies lightly and smoothly without any stickiness and residue.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Apply lightly on exposed skin 2~3 times

WARNINGS SECTION

If there are any abnormal symptoms or side effects such as red spots, swelling, or itching due to direct sunlight during or after using cosmetics. 2. Avoid using areas with wounds. 3. Precautions for storage and handling. 3.1) Keep out reach of children. 3.2) Keep it out of direct sunlight.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74997-0015-12023-01-30C16284748780-1f386c64a-145a-0266-e053-dadaa90a7c1aJ&J COMPANY - STOP-AGING PEPTIDE TONER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74997-0015-1W.SKIN TRIPLE CARE SUN17 g in 1 PACKAGESTICK171

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74997-0015W.SKIN TRIPLE CARE SUN (OCTOCRYLENE) STICK [J&J COMPANY]1Legacy NDC, 1 package rows20210509_c1c91698-5b21-1daa-e053-2a95a90ae1ac.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74997-001574997-0015-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
OCTOCRYLENE5A68WGF6WMACTIB

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
c1c91698-5b23-1daa-e053-2a95a90ae1acc1c91698-5b21-1daa-e053-2a95a90ae1ac2021-05-07WarningsExact identifier
spl id: c1c91698-5b23-1daa-e053-2a95a90ae1ac
spl set id: c1c91698-5b21-1daa-e053-2a95a90ae1ac

Reported adverse events (FAERS/openFDA)#

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