FDA.reportPublic FDA data

Sunscreen

Manufacturer
Private Label Select Ltd CO
Effective date
2020-02-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:11

Label at a glance#

ProductSunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Dosage and 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

OTC - 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 Section

OTC purpose sectionOTC purpose section

OTC Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

OTC Active IngredientsOTC Active Ingredients

Squeeze Tube Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Squeeze Tube ArtworkSqueeze Tube Artwork

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-216-372022-01-28C16284748780-1d6a99b39-a247-a426-e053-dadaa90af4c2Olita Mineral Sunscreen, SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-216-37Sunscreen88.7 g in 1 TUBEOINTMENT88.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-216SUNSCREEN (ZINC OXIDE SUNSCREEN) OINTMENT [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20200327_a1b2c6f3-8c33-2580-e053-2995a90a1e28.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62932-21662932-216-37

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
JOJOBA OIL724GKU717MIACT
SUNFLOWER OIL3W1JG795YIIACT
.BETA.-TOCOPHEROL9U6A490501IACT
WHITE WAX7G1J5DA97FIACT
SHEA BUTTERK49155WL9YIACT
ZINC OXIDESOI2LOH54ZACTIB
CASTOR OILD5340Y2I9GIACT
COCONUT OILQ9L0O73W7LIACT
OLIVE OIL6UYK2W1W1EIACT

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
a1b2c6f3-8c34-2580-e053-2995a90a1e28a1b2c6f3-8c33-2580-e053-2995a90a1e282020-02-01WarningsExact identifier
spl id: a1b2c6f3-8c34-2580-e053-2995a90a1e28
spl set id: a1b2c6f3-8c33-2580-e053-2995a90a1e28

Reported adverse events (FAERS/openFDA)#

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