FDA.reportPublic FDA data

SUN BUFF SPF 30 MINERAL SUNSCREEN

Manufacturer
SPF Ventures, LLC | Innovation Labs, Inc
Effective date
2025-09-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:14:50

Label at a glance#

ProductSUN BUFF SPF 30 MINERAL SUNSCREEN
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure8 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 sub exposure and as needed Reapply: After 80 minutes of swimming or sweating; Immediately after towel drying; At least every 2 hours Sub 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: L...

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

ZINC OXIDE 14.1%

TITANIUM DIOXIDE 8.05%

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 skin 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

When using this product 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 or irritation develops and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sub exposure and as needed
  • Reapply: After 80 minutes of swimming or sweating; Immediately after towel drying; At least every 2 hours

Sub 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 of age: ask a doctor

Other Information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

MICA

SILICA

BORON NITRIDE

DIMETHYLIMIDAZOLIDINONE RICE STARCH

IRON OXIDES (CI 77492)

LAUROYL LYSINE

SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL

TRIETHOXYCAPRYLYLSILANE

TITANIUM DIOXIDE (CI 77981)

GLYCERYL CAPRYLATE

IRON OXIDES (CI 77491)

ETHYL FERULATE

CARTHAMUS TINCTORIUS (SAFFLOWER) SEED OIL

BISABOLOL

IRON OXIDES (CI 77499)

ORYZA SATIVA (RICE) LIPIDS

GLYCERIN

CAPRYLHYDROXAMIC ACID

CAMELLIA SINENSIS EXTRACT

CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58274-030-01SUN BUFF SPF 30 MINERAL SUNSCREEN4 g in 1 TUBEPOWDER41

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58274-03058274-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
BORON NITRIDE2U4T60A6YDIACT
CHAMOMILEFGL3685T2XIACT
CAMELLIA SINENSIS LEAFW2ZU1RY8B0IACT
SILICAETJ7Z6XBU4IACT
CARTHAMUS TINCTORIUS (SAFFLOWER) SEED OIL65UEH262ISIACT
BISABOLOL24WE03BX2TIACT
GLYCERINPDC6A3C0OXIACT
LAUROYL LYSINE113171Q70BIACT
CI 77499XM0M87F357IACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
ETHYL FERULATE5B8915UELWIACT
ZINC OXIDESOI2LOH54ZACTIB
DIMETHYLIMIDAZOLIDINONE RICE STARCH43YT4X3R70IACT
CI 77492EX438O2MRTIACT
RICE BRAN OILLZO6K1506AIACT
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
MICAV8A1AW0880IACT
CI 774911K09F3G675IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT

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
SUN BUFF SPF 30 MINERAL SUNSCREENZINC OXIDE/TITANIUM DIOXIDESPF Ventures, LLC3f874062-ebab-8993-e063-6294a90abfc52025-09-24WarningsExact identifier
ndc (package): 58274-030-01
ndc (product): 58274-030
ndc11 (package): 58274003001
spl id: 3f874062-ebac-8993-e063-6294a90abfc5
spl set id: 3f874062-ebab-8993-e063-6294a90abfc5

Reported adverse events (FAERS/openFDA)#

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