PerfecTint Powder SPF 40

Manufacturer
Science of Skincare
Effective date
2025-01-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:52:15

Label at a glance#

ProductPerfecTint Powder SPF 40 All Shades
Active ingredientZINC OXIDE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 25%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Apply liberally 15 minutes before sun exposure

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product keep out of eyes.

Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

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

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.

Sun Protection Measures. Spending time in the sun increase 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-sleeve shirts, pants, hats, and sunglasses

Children under 6 months: Ask a doctor

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

OTC - QUESTIONS SECTION

Call Customer Care at (888)-804-4447

INACTIVE INGREDIENT SECTION

Mica, Dimethicone/Vinyl Dimethicone Crosspolymer, Calcium Sodium Borosilicate, Hydroxyapatite, Methyl Methacrylate Crosspolymer, Sodium Anisate, Lycopodium Clavatum Extract, Imperata Cylindrica Root Extract, Capryloyl Glycine, Glycerin, Triethoxycaprylylsiliane, Ironxe Oxides(CI 77491*, CI 77499*, CI77492*). *may contain one or more of these ingredients

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

69219-110 Cream Box69219-110 Cream Box69219-110 Ivory Box69219-110 Ivory Box69219-110 Beige Box69219-110 Beige Box69219-110 Deep Box69219-110 Deep Box69219-110 Bronze Box69219-110 Bronze Box69219-110 Bronze Cap69219-110 Bronze Cap69219-110 Beige Cap69219-110 Beige Cap69219-110 Deep Cap69219-110 Deep Cap69219-110 Ivory Cap69219-110 Ivory Cap69219-110 Cream Cap69219-110 Cream Cap69219-110 Jar69219-110 Jar69219-110 Component69219-110 Component

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69219-111-01PerfecTint Powder SPF 40All Shades3.5 g in 1 BOTTLE, PLASTICPOWDER3.54
69219-111-11PerfecTint Powder SPF 40All Shades1 in 1 BOXPOWDER14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69219-111PERFECTINT POWDER SPF 40 ALL SHADES (ZINC OXIDE) POWDER [SCIENCE OF SKINCARE]4Current NDC, 2 package rows20250112_bb26c010-299e-3dc5-e053-2995a90a2c89.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69219-11169219-111-01, 69219-111-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
PerfecTint Powder SPF 40 All ShadesZINC OXIDEScience of Skincarebb26c010-299e-3dc5-e053-2995a90a2c892025-01-09WarningsExact identifier
ndc (package): 69219-111-11
ndc (package): 69219-111-01
ndc (product): 69219-111
ndc11 (package): 69219011101
ndc11 (package): 69219011111
spl id: 2b4f67e8-6793-c22e-e063-6394a90ac9ac
spl set id: bb26c010-299e-3dc5-e053-2995a90a2c89

Reported adverse events (FAERS/openFDA)#

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