FDA.reportPublic FDA data

Baby Face Stick Mineral Sunscreen SPF 40

Manufacturer
Private Label Select Ltd CO
Effective date
2021-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:46:13

Label at a glance#

ProductBaby Face Stick Mineral Sunscreen SPF 40
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - Active Ingredient Section

OTC Active IngredientsOTC Active Ingredients

OTC - Purpose

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Inactive Ingredient Section

Inactive IngredientsInactive Ingredients

Indications and Usage

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Warnings Section

Warnings SectionWarnings Section

Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

Artwork - Inner Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Artwork InnerArtwork Inner

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-261-362023-01-30C16284748780-1f386c649-d34d-0266-e053-dadaa90a7c1aEarth Mama, Baby Face (Stick) Mineral Sunscreen, SPF 40

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-261-36Baby Face Stick Mineral Sunscreen SPF 401 in 1 CARTONSTICK11
62932-261-36Baby Face Stick Mineral Sunscreen SPF 4021 g in 1 CONTAINERSTICK211

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-261BABY FACE STICK MINERAL SUNSCREEN SPF 40 (SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 2 package rows20220101_d475423c-c0cb-4778-e053-2995a90a72ee.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
62932-26162932-261-36

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
WHITE WAX7G1J5DA97FIACT
CANDELILLA WAXWL0328HX19IACT
CARNAUBA WAXR12CBM0EIZIACT
SUNFLOWER OIL3W1JG795YIIACT
ALOE VERA LEAFZY81Z83H0XIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
SHEA BUTTERK49155WL9YIACT
COCOA BUTTER512OYT1CRRIACT
COCONUT OILQ9L0O73W7LIACT
.BETA.-TOCOPHEROL9U6A490501IACT
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
ZINC OXIDESOI2LOH54ZACTIB
.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
d475423c-c0cc-4778-e053-2995a90a72eed475423c-c0cb-4778-e053-2995a90a72ee2021-12-31WarningsExact identifier
spl id: d475423c-c0cc-4778-e053-2995a90a72ee
spl set id: d475423c-c0cb-4778-e053-2995a90a72ee

Reported adverse events (FAERS/openFDA)#

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