FDA.reportPublic FDA data

White Girl Sunscreen

Manufacturer
White Girl, LLC | Bath Concept Cosmetics (Dongguan) Co., Ltd.
Effective date
2017-01-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:48:29

Label at a glance#

ProductWhite Girl Sunscreen
Active ingredientOCTINOXATE, AVOBENZONE, OCTOCRYLENE, HOMOSALATE
Label structure3 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7%

Homosalate 3%

Octocrylene 6%

Avobenzone 2.5%

White Girl 30 SPF Sunscreen Active IngredientsWhite Girl 30 SPF Sunscreen Active Ingredients

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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 sun

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes.

Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If product is swallowed, get medical help

or contact a Poison Control Center right away.

Directions

  • apply liberally 15 minutes before sun exposure
  • reapply:
  • after 40 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours
  • Sun Protection Measures. Spending time in the sun increasess your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum spf of 30 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 a.m-2 p.m.
  • wear long-sleeve shirts, pants, hats, and sunglasses
  • children under 6 months: Ask a doctor

Other Information

protect this product from excessive heat and direct sun

White Girl Sunscreen Package Label DisplayWhite Girl Sunscreen Package Label Display

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70641-111-012020-01-31C16284748780-19d75b9d0-9d06-f424-e053-dadaa90a57ceWhite Girl Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70641-111-01White Girl Sunscreen100 g in 1 POUCHLOTION1004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70641-111WHITE GIRL SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE) LOTION [WHITE GIRL, LLC]4Legacy NDC, 1 package rows20170117_2f266c8f-7b7f-4ba5-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70641-11170641-111-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
AVOBENZONEG63QQF2NOXACTIB
OCTOCRYLENE5A68WGF6WMACTIB
HOMOSALATEV06SV4M95SACTIB
STEARETH-2153J3F32P58IACT

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
463e8172-8235-21b4-e054-00144ff88e882f266c8f-7b7f-4ba5-e054-00144ff88e882017-01-16Exact identifier
spl id: 463e8172-8235-21b4-e054-00144ff88e88
spl set id: 2f266c8f-7b7f-4ba5-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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