FDA.reportPublic FDA data

Sunscreen

Manufacturer
Private Label Select Ltd CO
Effective date
2019-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:02:40

Label at a glance#

ProductSunscreen
Active ingredientZINC OXIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reachKeep out of reach

OTC - Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

ActiveActive

Dosage

DOSAGE & ADMINISTRATION SECTION

DosageDosage

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

Indications and Usage

INDICATIONS & USAGE SECTION

IndicationsIndications

Purpose Section

OTC - PURPOSE SECTION

PurposePurpose

Warnings

WARNINGS SECTION

WarningsWarnings

Front Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront Label

Back Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Back LabelBack Label

Unit Carton Part 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Unit CartonUnit Carton

Unit Carton Part 2

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Unit CartonUnit Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-212-192021-01-29C16284748780-1ba0f9c33-4a58-a910-e053-dadaa90a0b85Think Operations, Think Baby SPF 30 Stick Canadian

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-212-19Sunscreen18.4 g in 1 CONTAINERSTICK18.41
62932-212-19Sunscreen1 in 1 CARTONSTICK11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-212SUNSCREEN (ZINC OXIDE SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 2 package rows20200101_9b064f84-ae7a-7848-e053-2995a90a1072.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
62932-21262932-212-19

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
ZINC OXIDESOI2LOH54ZACTIB
COCONUT OILQ9L0O73W7LIACT
SUNFLOWER OIL3W1JG795YIIACT
.BETA.-TOCOPHEROL9U6A490501IACT
CANDELILLA WAXWL0328HX19IACT
SHEA BUTTERK49155WL9YIACT
CASTOR OILD5340Y2I9GIACT
WHITE WAX7G1J5DA97FIACT
CARNAUBA WAXR12CBM0EIZIACT
COCOA BUTTER512OYT1CRRIACT
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
9b064cd0-a4cc-59ed-e053-2995a90a8ccd9b064f84-ae7a-7848-e053-2995a90a10722019-12-31WarningsExact identifier
spl id: 9b064cd0-a4cc-59ed-e053-2995a90a8ccd
spl set id: 9b064f84-ae7a-7848-e053-2995a90a1072

Reported adverse events (FAERS/openFDA)#

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