FDA.reportPublic FDA data

SUNSCREEN

Manufacturer
Private Label Select Ltd CO
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:46:18

Label at a glance#

ProductSUNSCREEN
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

Tubby Todd Play Mineral Sunstick Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

DosageDosage

Tubby Todd Play Mineral Sunstick, Warnings

WARNINGS SECTION

WarningsWarnings

Tubby Todd Play Mineral Sunstick Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Tubby Todd Play Mineral Sunstick Keep out of Reach

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of ReachKeep Out of Reach

OTC - PURPOSE SECTION

PurposePurpose

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Tubby Todd Label for Container

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

Tubby Todd Unit Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Unit CartonUnit Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-202-342023-07-28C16284748780-1ba0f9c33-49fb-a910-e053-dadaa90a0b85Tubby Todd Play Mineral Sunstick, SPF 30
62932-202-342022-01-04C16284748780-1ba0f9c33-49fb-a910-e053-dadaa90a0b85Tubby Todd Play Mineral Sunstick, SPF 30
62932-202-342021-01-29C16284748780-1ba0f9c33-49fb-a910-e053-dadaa90a0b85Tubby Todd Play Mineral Sunstick, SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-202-34SUNSCREEN1 in 1 CARTONSTICK12
62932-202-34SUNSCREEN14 g in 1 CONTAINERSTICK142

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-202SUNSCREEN (ZINC OXIDE SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]2Legacy NDC, 2 package rows20220105_9aca3bcb-db0c-2b46-e053-2995a90a11a0.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
62932-20262932-202-34

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

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
d4c4ed59-f03e-9d06-e053-2995a90a75d49aca3bcb-db0c-2b46-e053-2995a90a11a02022-01-04WarningsExact identifier
spl id: d4c4ed59-f03e-9d06-e053-2995a90a75d4
spl set id: 9aca3bcb-db0c-2b46-e053-2995a90a11a0

Reported adverse events (FAERS/openFDA)#

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