FDA.reportPublic FDA data

Sunscreen

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#

ProductSunscreen
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - Active Ingredient Section

OTC Active IngredientsOTC Active Ingredients

OTC - Purpose

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Indications and Usage

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Inactive Ingredient Section

Inactive IngredientsInactive Ingredients

Keep Out of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

Warnings Section

Warnings SectionWarnings Section

Artwork - Back Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Back LabelBack Label

Artwork - Front Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Artwork - FRONTArtwork - FRONT

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-255-422023-01-30C16284748780-1f386c649-a613-0266-e053-dadaa90a7c1aZinka, Mineral Zinc Oxide Face Stick SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-255-42Sunscreen18 g in 1 CONTAINERSTICK181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-255SUNSCREEN (ZINKA, MINERAL ZINC OXIDE FACE STICK SPF 30) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20211231_d4615204-e533-7d3c-e053-2995a90a0feb.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
62932-25562932-255-42

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

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
d4615204-e534-7d3c-e053-2995a90a0febd4615204-e533-7d3c-e053-2995a90a0feb2021-12-30WarningsExact identifier
spl id: d4615204-e534-7d3c-e053-2995a90a0feb
spl set id: d4615204-e533-7d3c-e053-2995a90a0feb

Reported adverse events (FAERS/openFDA)#

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