FDA.reportPublic FDA data

Brush on Block Mineral Powder Sunscreen Translucent

Manufacturer
SPF Ventures, LLC
Effective date
2024-12-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:44:04

Label at a glance#

ProductBrush on Block Mineral Powder Sunscreen Translucent
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure10 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 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. 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: • Limi...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 6%

Zinc Oxide 21%

Purpose

OTC - PURPOSE SECTION

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 aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INSTRUCTIONS FOR USE 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.
  • 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 10am - 2pm • Wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months: Ask a doctor

DOSAGE & ADMINISTRATION SECTION

Directions

Apply liberally 15 minutes before sun exposure
Reapply: • after 80 minutes of swimming or sweating • Immediately after towel drying • At least every 2 hours.
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 10am - 2pm • Wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months: Ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Bisabolol, Boron Nitride, Chamomile Flower Extract, Ethyl Ferulate, Hydroxyacetophenone, Iron Oxides, Lauroyl Lysine, Mica, Phenyl Trimethicone, Rice Bran Extract, Safflower Seed Oil, Silica, Sodium Dehydroacetate, Triethoxycaprylylsilane.

Other Information

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun.

Questions or Comments?

OTC - QUESTIONS SECTION

Contact our specialists at (800) 916-7690

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58274-011BRUSH ON BLOCK MINERAL POWDER SUNSCREEN TRANSLUCENT (TITANIUM DIOXIDE, ZINC OXIDE) POWDER [SPF VENTURES, LLC]2Unmatched20241229_f2b7ea75-738e-54a8-e053-2995a90a00d5.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58274-01158274-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIM
LAUROYL LYSINE113171Q70BIACT
SODIUM DEHYDROACETATE8W46YN971GIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
LEVOMENOL24WE03BX2TIACT
ETHYL FERULATE5B8915UELWIACT
MICAV8A1AW0880IACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
FERRIC OXIDE RED1K09F3G675IACT
RICE BRAN OILLZO6K1506AIACT
BORON NITRIDE2U4T60A6YDIACT
SAFFLOWER OIL65UEH262ISIACT
CHAMOMILEFGL3685T2XIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
45fff1f6-8c22-f3a2-e063-6394a90a3f0ef2b7ea75-738e-54a8-e053-2995a90a00d52025-12-15WarningsExact identifier
spl set id: f2b7ea75-738e-54a8-e053-2995a90a00d5

Reported adverse events (FAERS/openFDA)#

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