FDA.reportPublic FDA data

Sunscreen

Manufacturer
Private Label Select Ltd CO
Effective date
2020-07-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:43

Label at a glance#

ProductSunscreen
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTSACTIVE INGREDIENTS

DOSAGE AND ADMIN.

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

OTC- KEEP OUT OF REACH

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC KEEP OUT OF REACHOTC KEEP OUT OF REACH

OTC-PURPOSE

OTC - PURPOSE SECTION

PUPOSEPUPOSE

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

WARNINGS SECTION

WARNINGSWARNINGS

BACK LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Back LabelBack Label

FRONT LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FRONT LABELFRONT LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-219-262022-01-28C16284748780-1d6a99b39-91c5-a426-e053-dadaa90af4c2Suntegrity, Mineral Sun Stick, SPF 30 - Tinted Light

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-219-26Sunscreen46 g in 1 CONTAINERSTICK461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-219SUNSCREEN (ZINC OXIDE SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20200717_aa97bab0-5885-3e6c-e053-2a95a90a4330.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62932-21962932-219-26

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
COCOA BUTTER512OYT1CRRIACT
CASTOR OILD5340Y2I9GIACT
ALOE VERA LEAFZY81Z83H0XIACT
.DELTA.-TOCOPHEROLJU84X1II0NIACT
FERRIC OXYHYDROXIDE87PZU03K0KIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
CANDELILLA WAXWL0328HX19IACT
CARNAUBA WAXR12CBM0EIZIACT
MICAV8A1AW0880IACT
FERRIC OXIDE RED1K09F3G675IACT
WHITE WAX7G1J5DA97FIACT
SUNFLOWER OIL3W1JG795YIIACT
SHEA BUTTERK49155WL9YIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
.BETA.-TOCOPHEROL9U6A490501IACT

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
aa97bab0-5886-3e6c-e053-2a95a90a4330aa97bab0-5885-3e6c-e053-2a95a90a43302020-07-16WarningsExact identifier
spl id: aa97bab0-5886-3e6c-e053-2a95a90a4330
spl set id: aa97bab0-5885-3e6c-e053-2a95a90a4330

Reported adverse events (FAERS/openFDA)#

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