FDA.reportPublic FDA data

SUNSCREEN

Manufacturer
Private Label Select Ltd CO
Effective date
2020-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:21

Label at a glance#

ProductSUNSCREEN
Active ingredientZINC OXIDE
Label structure5 sections

Label contents#

Full prescribing information#

Tubby Todd Play Mineral Sunstick Keep out of Reach

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

OTC - ACTIVE INGREDIENT SECTION

OTC Active IngredientsOTC Active Ingredients

Tubby Todd Label for Container

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

Tubby Todd Unit Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-250-342022-01-28C16284748780-1d6a99b3a-01c6-a426-e053-dadaa90af4c2Tubby Todd Play Mineral Sunstick, SPF 30 (Maisonette)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-250-34SUNSCREEN1 in 1 CARTONSTICK11
62932-250-34SUNSCREEN14 g in 1 CONTAINERSTICK141

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-250SUNSCREEN (ZINC OXIDE SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 2 package rows20210101_b7c7cb59-6083-3fd7-e053-2a95a90af558.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
62932-25062932-250-34

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
ALOE VERA LEAFZY81Z83H0XIACT
.BETA.-TOCOPHEROL9U6A490501IACT
ZINC OXIDESOI2LOH54ZACTIB
CANDELILLA WAXWL0328HX19IACT
CARNAUBA WAXR12CBM0EIZIACT
COCOA BUTTER512OYT1CRRIACT
COCONUT OILQ9L0O73W7LIACT
WHITE WAX7G1J5DA97FIACT
SUNFLOWER OIL3W1JG795YIIACT
SHEA BUTTERK49155WL9YIACT
CASTOR OILD5340Y2I9GIACT

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
b7c7d5cd-a29a-8898-e053-2995a90a482cb7c7cb59-6083-3fd7-e053-2a95a90af5582020-04-01Exact identifier
spl id: b7c7d5cd-a29a-8898-e053-2995a90a482c
spl set id: b7c7cb59-6083-3fd7-e053-2a95a90af558

Reported adverse events (FAERS/openFDA)#

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