FDA.reportPublic FDA data

Tinted Sunscreen

Manufacturer
Private Label Select Ltd CO
Effective date
2020-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:08

Label at a glance#

ProductTinted Sunscreen
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

DosageDosage

Warnings Section

WarningsWarnings

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

Indications and Usage

INDICATIONS & USAGE SECTION

IndicationsIndications

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reachKeep out of reach

OTC - Purpose

OTC - PURPOSE SECTION

PurposePurpose

OTC - Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

ActiveActive

Label Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Unit Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Unit CartonUnit Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-213-362022-01-28C16284748780-1d6a99b39-39a3-a426-e053-dadaa90af4c2Earth Mama Lady Face Mineral Sunscreen, SPF 40 - Light/Medium

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-213-36Tinted Sunscreen1 in 1 CARTONSTICK11
62932-213-36Tinted Sunscreen21 g in 1 TUBESTICK211

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-213TINTED SUNSCREEN (ZINC OXIDE TINTED SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 2 package rows20200327_9b06f711-289e-03a1-e053-2995a90a783c.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
62932-21362932-213-36

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
COCONUT OILQ9L0O73W7LIACT
WHITE WAX7G1J5DA97FIACT
CANDELILLA WAXWL0328HX19IACT
CARNAUBA WAXR12CBM0EIZIACT
SUNFLOWER OIL3W1JG795YIIACT
SHEA BUTTERK49155WL9YIACT
ALOE VERA LEAFZY81Z83H0XIACT
ZINC OXIDESOI2LOH54ZACTIB
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
COCOA BUTTER512OYT1CRRIACT
.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
9b06f711-289f-03a1-e053-2995a90a783c9b06f711-289e-03a1-e053-2995a90a783c2020-01-01WarningsExact identifier
spl id: 9b06f711-289f-03a1-e053-2995a90a783c
spl set id: 9b06f711-289e-03a1-e053-2995a90a783c

Reported adverse events (FAERS/openFDA)#

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