Mineral Tinted Face Sunscreen SPF 30 - Medium/ Dark

Manufacturer
Unsun Cosmetics | Pack On Demand
Effective date
2022-03-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:48:54

Label at a glance#

ProductMineral Tinted Face Sunscreen SPF 30 - Light/ Medium
Active ingredientZINC OXIDE, Titanium Dioxide
Label structure9 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

Adults and children over 6 months of age: Apply liberally and evenly 15 minutes before sun exposure. Reapply after 80 minutes of swimming or perspiring heavily or immediately after towel drying or washing, at least every 2 hours. Children under 6 months of age: Ask a doctor. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly u...

Storage and handling

protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Medicinal ingredientsPurpose
Titanium dioxide 5.5%Sunscreen
Zinc oxide 6.5%Sunscreen

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

Warnings

WARNINGS SECTION

Skin Cancer/Skin Aging Alert

SPL UNCLASSIFIED SECTION

Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging For external use only. Do not use on damaged or broken skin. When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. 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, call a poison control center or get medical help right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 6 months of age: Apply liberally and evenly 15 minutes before sun exposure. Reapply after 80 minutes of swimming or perspiring heavily or immediately after towel drying or washing, at least every 2 hours. Children under 6 months of age: Ask a doctor. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m.– 2 p.m. Wear long-sleeved shirts, pants, hats, and sunglasses.

Non-medicinal ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Caprylic/Capric Triglyceride, Isoamyl Laurate, Glycerin, Polyglyceryl-2 Sesquioleate, Coconut Alkanes, Polyglyceryl-3 Ricinoleate, Crambe Abyssinica (Abyssinian) Seed Oil, Sorbitan Sesquioleate, Polyhydroxystearic Acid, Heptyl Undecylenate, Alumina, Stearic Acid, Magnesium Sulfate, Sodium Chloride, Coco-Caprylate/Caprate, Benzyl Alcohol, Butyrospermum Parkii (Shea) Butter, Carthamus Tinctorius (Safflower) Seed Oil, Aloe Barbadensis Leaf Juice, Beeswax/Cera Alba/Cire d' Abeille, Cocos Nucifera (Coconut) Oil, Cucumis Sativus (Cucumber) Fruit Extract, Olea Europaea (Olive) Fruit Oil, Ascorbic Acid, Beta Vulgaris (Beet) Root Extract, Citric Acid, Citrus Aurantium Amara (Bitter Orange) Fruit Extract, Citrus Aurantium Sinensis Peel Extract, Citrus Reticulata (Tangerine) Fruit Extract, Glycine Soja (Soybean) Oil, Hydrolyzed Corn Starch, Lactic Acid, p-Anisic Acid, Tocopherol, Triethoxycaprylylsilane, Iron Oxides (CI 77491, CI 77492, CI 77499).

Other information

STORAGE AND HANDLING SECTION

  • protect this product from excessive heat and direct sun

PRINCIPAL DISPLAY PANEL - 50 mL Tube Label - Light Medium

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

unsun™

MINERAL TINTED
FACE SUNSCREEN
LOTION

30

BROAD SPECTRUM
SPF 30

WATER RESISTANT
(80 MINUTES)

NPN xxxxx

LIGHT - MEDIUM

1.7 FL OZ | 50 mL

PRINCIPAL DISPLAY PANEL - 50 mL Tube Label - Light Medium
PRINCIPAL DISPLAY PANEL - 50 mL Tube Label - Light Medium

PRINCIPAL DISPLAY PANEL - 50 mL Tube Label - Medium Dark

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

unsun™

MINERAL TINTED
FACE SUNSCREEN
LOTION

30

BROAD SPECTRUM
SPF 30

WATER RESISTANT
(80 MINUTES)

NPN xxxxx

MEDIUM - DARK

1.7 FL OZ | 50 mL

PRINCIPAL DISPLAY PANEL - 50 mL Tube Label - Medium Dark
PRINCIPAL DISPLAY PANEL - 50 mL Tube Label - Medium Dark

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73455-011-282025-01-30C16284748780-12cef2736-ac47-d83d-e063-dadaa90ab31fMineral Tinted Face Sunscreen SPF 30
73455-111-302025-01-30C16284748780-12cef2736-ac47-d83d-e063-dadaa90ab31fMineral Tinted Face Sunscreen SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73455-011-28Mineral Tinted Face Sunscreen SPF 30 - Light/ Medium50 mL in 1 TUBECREAM502
73455-011-28Mineral Tinted Face Sunscreen SPF 30 - Light/ Medium1 in 1 BOXCREAM12
73455-111-30Mineral Tinted Face Sunscreen SPF 30 - Medium/ Dark50 mL in 1 TUBECREAM502
73455-111-30Mineral Tinted Face Sunscreen SPF 30 - Medium/ Dark1 in 1 BOXCREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73455-011MINERAL TINTED FACE SUNSCREEN SPF 30 - LIGHT/ MEDIUM (ZINC OXIDE AND TITANIUM DIOXIDE) CREAM MINERAL TINTED FACE SUNSCREEN SPF 30 - MEDIUM/ DARK (ZINC OXIDE AND TITANIUM DIOXIDE) CREAM [UNSUN COSMETICS]2Legacy NDC, 2 package rows20220325_a2a7b6f0-8f2c-4654-977d-955f535d7ca4.zip
73455-111MINERAL TINTED FACE SUNSCREEN SPF 30 - LIGHT/ MEDIUM (ZINC OXIDE AND TITANIUM DIOXIDE) CREAM MINERAL TINTED FACE SUNSCREEN SPF 30 - MEDIUM/ DARK (ZINC OXIDE AND TITANIUM DIOXIDE) CREAM [UNSUN COSMETICS]2Legacy NDC, 2 package rows20220325_a2a7b6f0-8f2c-4654-977d-955f535d7ca4.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73455-01173455-011-28
73455-11173455-111-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
880b7e4c-d962-466f-a29e-76d03df93f72a2a7b6f0-8f2c-4654-977d-955f535d7ca42022-03-24WarningsExact identifier
spl id: 880b7e4c-d962-466f-a29e-76d03df93f72
spl set id: a2a7b6f0-8f2c-4654-977d-955f535d7ca4

Reported adverse events (FAERS/openFDA)#

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