2WINS GLOWING SKIN TINTED MOISTURIZER SUNSCREEN MEDIUM

Manufacturer
IKISTAR TEKSTIL DIZAYN LIMITED SIRKETI | MADDY GLOBAL LLC
Effective date
2026-03-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:58:55

Label at a glance#

Product2WINS GLOWING SKIN TINTED MOISTURIZER SUNSCREEN LIGHT
Active ingredientOCTISALATE
Label structure11 sections

Indications and uses

• helps prevent sunburn • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

• apply liberally 15 minutes before sun exposure • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours • children under 6 months: Ask a doctor Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging caused by the sun. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF 15 or higher and...

Label contents#

Full prescribing information#

Aktive ingredients

OTC - ACTIVE INGREDIENT SECTION

Octisalate 5%

Uses

INDICATIONS & USAGE SECTION

• helps prevent sunburn

• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• apply liberally 15 minutes before sun exposure
• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours
• children under 6 months: Ask a doctor

Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging caused by the sun. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF 15 or higher and other sun protection measures including:
• limit time in the sun, especially from 10 a.m. – 2 p.m.
• wear long-sleeve shirts, pants, hats, and sunglasses

Warnings

WARNINGS SECTION

For external use only

Purpose

OTC - PURPOSE SECTION

Sunscreen

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cyclopentasiloxane, Dimethicone, Propylene Glycol, Alpha-Arbutin, Niacinamide, Disteardimonium Hectorite, PEG-10 Dimethicone, Trimethylsiloxysilicate, Polysilicone-11, Laureth-12, Mica, Lauroyl Lysine, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, Talc, Glycerin, Sodium Hyaluronate, Ceramide NP, Ceramide AP, Ceramide EOP, Sodium PCA, Urea, Allantoin, Fructose, Sodium Lactate, Maltose, Trehalose, Phytosterols, Phytosphingosine, Glucose, Pentylene Glycol, Hydrogenated Phosphatidylcholine, Butylene Glycol, Tocopheryl Acetate, Triethoxycaprylylsilane, Isononyl Isononanoate, Ethylene/Propylene/Styrene Copolymer, Sorbitan Oleate, Sodium Chloride, Citric Acid, Sodium Hydroxide, Ethylhexylglycerin, Phenoxyethanol, Iron Oxides (CI 77499, CI 77491, CI 77492), Titanium Dioxide (CI 77891).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tintedtinted

GLOWING SKIN

TINTED MOISTURIZER SUNSCREEN

Broad Spectrum SPF 30

CERAMIDE COMPLEX
ARBUTIN
HYALURONIC ACID

2 WINS MAKE-UP

Net 50 mL (1.69 fl oz)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tinted1tinted1tinted1tinted1

GLOWING SKIN

TINTED MOISTURIZER SUNSCREEN

Broad Spectrum SPF 30

CERAMIDE COMPLEX
ARBUTIN
HYALURONIC ACID

2 WINS MAKE-UP

Net 50 mL (1.69 fl oz)

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

Products#

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

DailyMed product names page 1 of 2 · 52 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87524-00287524-002-01, 87524-002-02
87524-00187524-001-01, 87524-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 3 · 98 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
504c2f6e-4d76-19bb-e063-6394a90a417f4ca7eac6-85ef-d684-e063-6294a90a70582026-04-25WarningsExact identifier
spl set id: 4ca7eac6-85ef-d684-e063-6294a90a7058

Reported adverse events (FAERS/openFDA)#

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