FDA.reportPublic FDA data

John Wayne Cancer Foundation Mineral Sunscreen Facestick SPF 30

Manufacturer
Private Label Select Ltd CO
Effective date
2021-12-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:46:08

Label at a glance#

ProductJohn Wayne Cancer Foundation Mineral Sunscreen Facestick SPF 30
Active ingredientZINC OXIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - Active Ingredient Section

OTC Active IngredientsOTC Active Ingredients

OTC - Purpose Section

OTC PurposeOTC Purpose

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Directions and AdministrationDirections and Administration

Inactive Ingredient Section

Inactive IngredientsInactive Ingredients

Indications and Usage

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Warnings Section

Warnings SectionWarnings Section

Artwork - Back Label #1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Artwork Back OneArtwork Back One

Artwork - Back #2

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Artwork Back TwoArtwork Back Two

Artwork - Back Three

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Artwork Back ThreeArtwork Back Three

Artwork - Front Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Artwork - FRONTArtwork - FRONT

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-256-332023-01-30C16284748780-1f386c64a-32ef-0266-e053-dadaa90a7c1aX3EMBrands, LLC John Wayne Cancer Foundation Mineral Sunscreen Facestick SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-256-33John Wayne Cancer Foundation Mineral Sunscreen Facestick SPF 3014 g in 1 CONTAINERSTICK141

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-256JOHN WAYNE CANCER FOUNDATION MINERAL SUNSCREEN FACESTICK SPF 30 (SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20211231_d46213d2-2048-74e3-e053-2a95a90a7fc1.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
62932-25662932-256-33

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUNFLOWER OIL3W1JG795YIIACT
WHITE WAX7G1J5DA97FIACT
CANDELILLA WAXWL0328HX19IACT
SHEA BUTTERK49155WL9YIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
.BETA.-TOCOPHEROL9U6A490501IACT
CARNAUBA WAXR12CBM0EIZIACT
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
.DELTA.-TOCOPHEROLJU84X1II0NIACT
COCOA BUTTER512OYT1CRRIACT
COCONUT OILQ9L0O73W7LIACT
ZINC OXIDESOI2LOH54ZACTIB
CASTOR OILD5340Y2I9GIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
d46213d2-2049-74e3-e053-2a95a90a7fc1d46213d2-2048-74e3-e053-2a95a90a7fc12021-12-30WarningsExact identifier
spl id: d46213d2-2049-74e3-e053-2a95a90a7fc1
spl set id: d46213d2-2048-74e3-e053-2a95a90a7fc1

Reported adverse events (FAERS/openFDA)#

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