Derma Soleil Tinted Mineral Age-Free Facial BB Broad Spectrum SPF 30 Sunscreen

Manufacturer
Derma Soleil | Deserving Health International Corp
Effective date
2023-05-24
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:30:17

Label at a glance#

ProductDerma Soleil Mineral Broad Spectrum SPF 30 Sunscreen
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure1 sections

Label contents#

Full prescribing information#

Derma Soleil Mineral Broad Spectrum Sunscreen Lotion SPF 30

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Derma Soleil Mineral Broad Spectrum Sunscreen SPF 30Derma Soleil Mineral Broad Spectrum Sunscreen SPF 30

OTC - PURPOSE SECTION

Sunscreen

OTC - ACTIVE INGREDIENT SECTION

Micronized Zinc Oxide 11%

Micronized Titanium Dioxide 8%

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

INDICATIONS & USAGE SECTION

The sun may cause sunburn, premature aging of the skin and skin cancer. Avoiding the sun, wearing protective clothing and regular use of sunscreens over the years reduces the chance of these harmful effects.

Helps prevent sunburn

If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by sun

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and consult a doctor if rash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure

Reapply

After 40 minutes of swimming or sweating

immediately after towel drying

at least every 2 hours

Children under 6 months of age: ask a doctor

INACTIVE INGREDIENT SECTION

Water, Coco-Caprylate, Dicaprylyl Carbonate, Lauryl Glucoside,

Polyglyceryl-2 Dipolyhydroxystearate, Glycerin, Microcrystalline Cellulose,

Cellulose Gum, Green Tea Extract, DL-Panthenol, Sodium Ascorbyl Phosphate,

D-alpha Tocopheryl Acetate, Phytic Acid, Triethoxycaprylylsilane, Polyhydroxystearic Acid,

Xanthan Gum, Benzyl Alcohol, Ethylhexylglycerin, D-alpha Tocopherol

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69711-34069711-340-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
0cdb2470-91a8-6ce8-e063-6394a90acf028b116370-13b1-f6f4-e053-2995a90a066c2023-12-19WarningsExact identifier
spl set id: 8b116370-13b1-f6f4-e053-2995a90a066c

Reported adverse events (FAERS/openFDA)#

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