Vertra Pearl White Face Stick SPF 50

Manufacturer
Eai-jr 286, Inc
Effective date
2025-10-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:38:11

Label at a glance#

ProductVertra Pearl White Face Stick SPF 50
Active ingredientPADIMATE O, TITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

PADIMATE O 7% Sunscreen

TITANIUM DIOXIDE 17% Sunscreen

OTC - PURPOSE SECTION

Uses

  • Helps prevent sunburn
  • If used as directed with other sun protection (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.
  • Higher SPF gives more sunburn protection
  • Retains SPF after 80 minutes activity in the water, sweating, or perspiring.
  • Provides high protection against sunburn

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

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if:

Rash or irritation develops and lasts

WARNINGS SECTION

Warnings

Do not use:

  • On damaged or broken skin

When using this product:

  • keep out of eyes. Rinse with water to remove
  • For external use only

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally and generously 15 minutes before sun exposure and at least every 2 hours
  • Children under 6 months of age: ask a doctor.
  • 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 your time in the sun, especially from 10 a.m. – 2 p.m.
  • wear long-sleeved shirts, pants, hats, and sunglasses
  • Reapply:
  • After 80 minutes of swimming or sweating
  • Immediately after towel drying
  • at least every 2 hours

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Hexyldecyl Isostearate, Mica, Synthetic Wax, Paraffin, Ozokerite, Polyglyceryl-2 Oleate, Aluminum Hydroxide, Stearic Acid, Ethylene/Propylene Copolymer, Tocopherol, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

vertra

50 +

Pearl White Face Stick

Mineral Based Foundation

Broad Spectrum SPF 50+

Water Resistant (80 Minutes)

10.5g NET WT 0.37 OZ

Pearl White artPearl White art

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130889297073276GTIN-13: 0889297073276
EAN-13: 0889297073276
GTIN-12: 889297073276
UPC-A: 889297073276
GTIN storage (14 digits): 00889297073276
pearl white art - fda reg.jpg
QR code linkQR Codewww.vertra.com/pearl white art - fda reg.jpg

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71014-025-01Vertra Pearl White Face Stick SPF 5010.5 g in 1 CARTONSTICK10.54

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71014-02571014-025-01

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32024-10-22full-release2026-06-01 00:28:35

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
Vertra Pearl White Face Stick SPF 50PADIMATE O, TITANIUM DIOXIDEEai-jr 286, Incb69a75e0-8724-35ae-e053-2a95a90a5f342025-10-07WarningsExact identifier
ndc (package): 71014-025-01
ndc (product): 71014-025
ndc11 (package): 71014002501
spl id: 40976326-e3d0-25ce-e063-6294a90a9224
spl set id: b69a75e0-8724-35ae-e053-2a95a90a5f34

Reported adverse events (FAERS/openFDA)#

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