FDA.reportPublic FDA data

Tinted Mineral Face Sunscreen Stick - Creme

Manufacturer
Private Label Select Ltd CO
Effective date
2020-12-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:01

Label at a glance#

ProductTinted Mineral Face Sunscreen Stick - Creme
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Warnings Section

WarningWarning

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

Indications and Usage

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

OTC - Keep out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

OTC Purpose

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

OTC Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

OTC Active IngredientsOTC Active Ingredients

Artwork - Front and Back Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-221-332022-01-28C16284748780-1d6a99b3a-01e7-a426-e053-dadaa90af4c2Beauty By Earth Tinted Mineral Face Sunscreen Stick - Creme

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-221-33Tinted Mineral Face Sunscreen Stick - Creme14 g in 1 CONTAINERSTICK141

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-221TINTED MINERAL FACE SUNSCREEN STICK - CREME STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20201229_b78b3e97-e3b6-59e4-e053-2995a90a580c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62932-22162932-221-33

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CASTOR OILD5340Y2I9GIACT
FERRIC OXIDE RED1K09F3G675IACT
CARNAUBA WAXR12CBM0EIZIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
.BETA.-TOCOPHEROL9U6A490501IACT
SUNFLOWER OIL3W1JG795YIIACT
CANDELILLA WAXWL0328HX19IACT
ZINC OXIDESOI2LOH54ZACTIB
SHEA BUTTERK49155WL9YIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
COCOA BUTTER512OYT1CRRIACT
WHITE WAX7G1J5DA97FIACT
MICAV8A1AW0880IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
FERRIC OXYHYDROXIDE87PZU03K0KIACT
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
.DELTA.-TOCOPHEROLJU84X1II0NIACT

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
b78b3e97-e3b7-59e4-e053-2995a90a580cb78b3e97-e3b6-59e4-e053-2995a90a580c2020-12-28WarningsExact identifier
spl id: b78b3e97-e3b7-59e4-e053-2995a90a580c
spl set id: b78b3e97-e3b6-59e4-e053-2995a90a580c

Reported adverse events (FAERS/openFDA)#

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