FDA.reportPublic FDA data

In Your Face Mineral Tint SPF 31

Manufacturer
Kabana Skin Care
Effective date
2024-10-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:51:15

Label at a glance#

ProductIn Your Face Mineral Tint SPF 31
Active ingredientZINC OXIDE
Label structure1 sections

Label contents#

Full prescribing information#

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

InYourFace Mineral TInt SPF 31InYourFace Mineral TInt SPF 31

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 25%

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
DOSAGE & ADMINISTRATION SECTION
  • Apply liberally 15 minutes before sun exposure
  • Use a water resistant sunscreen if swimming or sweating
  • Reapply at least every 2 hours

Directions

INSTRUCTIONS FOR USE SECTION

  • Children under 6 months. Ask a doctor.
  • Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early 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 AM - 2 PM.
  • Wear long-sleeved shirts, pants, hats and sunglasses
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 immediately.

Warnings

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

Stop use and ask a doctor if rash occurs

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Artesian Spring Water, Extra Virgin Olive Oil*, Jojoba Oil*, Vegetable Glycerin*, Shea Butter*, Vgetable Emulsifying Wax NF+, Vitamin E, Iron Oxides. *Organic

Other Information

OTHER SAFETY INFORMATION

  • Protect this product from excessive heat and direct sun

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
73369-160173369-1601-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
FERRIC OXIDE RED1K09F3G675IACT
OLIVE OIL6UYK2W1W1EIACT
ZINC OXIDESOI2LOH54ZACTIB
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERINPDC6A3C0OXIACT
SHEA BUTTERK49155WL9YIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
POLYSORBATE 60CAL22UVI4MIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
JOJOBA OIL724GKU717MIACT

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
31cf4721-5010-7701-e063-6394a90a449b021a2841-fe1a-808c-e063-6294a90aedfa2025-04-02WarningsExact identifier
spl set id: 021a2841-fe1a-808c-e063-6294a90aedfa

Reported adverse events (FAERS/openFDA)#

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