FDA.reportPublic FDA data

Lady Face Mineral Sunscreen, SPF 40 - Medium/Dark

Manufacturer
Private Label Select Ltd CO
Effective date
2021-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:46:08

Label at a glance#

ProductLady Face Mineral Sunscreen, SPF 40 - Medium/Dark
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Warnings Section

Warnings SectionWarnings Section

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

Indications and Usage

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - Purpose

OTC - PURPOSE SECTION

OTC Active IngredientsOTC Active Ingredients

OTC - Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient SectionActive Ingredient Section

Label Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

Unit Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Artwork - Unit CartonArtwork - Unit Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-258-362023-01-30C16284748780-1f386c649-c3f3-0266-e053-dadaa90a7c1aEarth Mama Lady Face Mineral Sunscreen, SPF 40 - Medium/Dark

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-258-36Lady Face Mineral Sunscreen, SPF 40 - Medium/Dark21 g in 1 CONTAINERSTICK211
62932-258-36Lady Face Mineral Sunscreen, SPF 40 - Medium/Dark1 in 1 CARTONSTICK11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-258LADY FACE MINERAL SUNSCREEN, SPF 40 - MEDIUM/DARK (ZINC OXIDE TINTED SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 2 package rows20211231_d464ad3a-0b4d-bcdb-e053-2995a90a534f.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62932-25862932-258-36

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
FERRIC OXYHYDROXIDE87PZU03K0KIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
.DELTA.-TOCOPHEROLJU84X1II0NIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
COCOA BUTTER512OYT1CRRIACT
.BETA.-TOCOPHEROL9U6A490501IACT
COCONUT OILQ9L0O73W7LIACT
WHITE WAX7G1J5DA97FIACT
CANDELILLA WAXWL0328HX19IACT
CARNAUBA WAXR12CBM0EIZIACT
SUNFLOWER OIL3W1JG795YIIACT
SHEA BUTTERK49155WL9YIACT
ALOE VERA LEAFZY81Z83H0XIACT
ZINC OXIDESOI2LOH54ZACTIB
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT

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
d464a42a-2fb5-6c79-e053-2a95a90a0b9bd464ad3a-0b4d-bcdb-e053-2995a90a534f2021-01-01WarningsExact identifier
spl id: d464a42a-2fb5-6c79-e053-2a95a90a0b9b
spl set id: d464ad3a-0b4d-bcdb-e053-2995a90a534f

Reported adverse events (FAERS/openFDA)#

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