FDA.reportPublic FDA data

SUNSCREEN

Manufacturer
Private Label Select Ltd CO
Effective date
2019-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:43

Label at a glance#

ProductSUNSCREEN
Active ingredientZINC OXIDE
Label structure7 sections

Label contents#

Full prescribing information#

Warnings Z24 SPF 30 Sun Stick

WARNINGS SECTION

Warnings Z24 SPF 30 Sun StickWarnings Z24 SPF 30 Sun Stick

Inactive Ingredients Section Z24 SPF 30 Sun Stick

INACTIVE INGREDIENT SECTION

Inactive Ingredients Z24 SPF 30 Sun StickInactive Ingredients Z24 SPF 30 Sun Stick

Indications & Usage Section Z24 SPF 30 Sun Stick

INDICATIONS & USAGE SECTION

Indications Usage Section Z24 SPF 30 Sun StickIndications Usage Section Z24 SPF 30 Sun Stick

Dosage & Administration Z24 SPF 30 Sun Stick

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration Z24 SPF 30 Sun StickDosage & Administration Z24 SPF 30 Sun Stick

OTC - Purpose Z24 SPF 30 Sun Stick

OTC - PURPOSE SECTION

OTC - Purpose Z24 SPF 30 Sun StickOTC - Purpose Z24 SPF 30 Sun Stick

OTC Active Ingedients Z24 SPF 30 Sunstick

OTC - ACTIVE INGREDIENT SECTION

OTC Active Ingedients Z24 SPF 30 SunstickOTC Active Ingedients Z24 SPF 30 Sunstick

Z24 SPF 30 Sun Stick

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Z24 SPF 30 Sun StickZ24 SPF 30 Sun Stick

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-192-192021-01-29C16284748780-1ba0f9c33-3bac-a910-e053-dadaa90a0b85Z24 SPF 30 Sun Stick

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-192-19SUNSCREEN19 g in 1 TUBESTICK191

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-192SUNSCREEN (ZINC OXIDE SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20190619_8b9c125f-fe28-bb03-e053-2995a90a09c2.zip

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
62932-19262932-192-19

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
CASTOR OILD5340Y2I9GIACT
SUNFLOWER OIL3W1JG795YIIACT
ZINC OXIDESOI2LOH54ZACTIB
COCONUT OILQ9L0O73W7LIACT
YELLOW WAX2ZA36H0S2VIACT
CANDELILLA WAXWL0328HX19IACT
SHEA BUTTERK49155WL9YIACT
COCOA BUTTER512OYT1CRRIACT
CARNAUBA WAXR12CBM0EIZIACT
TOCOPHEROLR0ZB2556P8IACT
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
8b9c125f-fe29-bb03-e053-2995a90a09c28b9c125f-fe28-bb03-e053-2995a90a09c22019-06-18WarningsExact identifier
spl id: 8b9c125f-fe29-bb03-e053-2995a90a09c2
spl set id: 8b9c125f-fe28-bb03-e053-2995a90a09c2

Reported adverse events (FAERS/openFDA)#

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