FDA.reportPublic FDA data

Sunscreen

Manufacturer
Private Label Select Ltd CO
Effective date
2020-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:20

Label at a glance#

ProductSunscreen
Active ingredientZINC OXIDE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

OTC Active IngredientsOTC Active Ingredients

OTC - KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC Keep Out Of Reach Of ChildrenOTC Keep Out Of Reach Of Children

OTC - PURPOSE

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

ARTWORK (BACK LABEL NO. 1)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ARTWORK - BACKARTWORK - BACK

ARTWORK (BACK LABEL NO. 2)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ARTWORK - BACKARTWORK - BACK

ARTWORK (FRONT LABEL)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

ARTWORK (BACK LABEL NO. 3)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ARTWORK - BACKARTWORK - BACK

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-243-422022-01-28C16284748780-1d6a99b3a-01ae-a426-e053-dadaa90af4c2Rinse Bath & Body SPF 30 Unscented Sunstick

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-243-42Sunscreen18 g in 1 CONTAINERSTICK181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-243SUNSCREEN (ZINC OXIDE SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20210101_b7c56c15-c1ec-ab0d-e053-2995a90a7e5f.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
62932-24362932-243-42

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
SUNFLOWER OIL3W1JG795YIIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
COCONUT OILQ9L0O73W7LIACT
ALOE VERA LEAFZY81Z83H0XIACT
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
.DELTA.-TOCOPHEROLJU84X1II0NIACT
SHEA BUTTERK49155WL9YIACT
ZINC OXIDESOI2LOH54ZACTIB
WHITE WAX7G1J5DA97FIACT
CANDELILLA WAXWL0328HX19IACT
COCOA BUTTER512OYT1CRRIACT
CARNAUBA WAXR12CBM0EIZIACT
CASTOR OILD5340Y2I9GIACT
.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
b7c56c15-c1ed-ab0d-e053-2995a90a7e5fb7c56c15-c1ec-ab0d-e053-2995a90a7e5f2020-12-31Exact identifier
spl id: b7c56c15-c1ed-ab0d-e053-2995a90a7e5f
spl set id: b7c56c15-c1ec-ab0d-e053-2995a90a7e5f

Reported adverse events (FAERS/openFDA)#

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