FDA.reportPublic FDA data

SUNSCREEN

Manufacturer
Private Label Select Ltd CO
Effective date
2020-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:21

Label at a glance#

ProductSUNSCREEN
Active ingredientZINC OXIDE
Label structure4 sections

Label contents#

Full prescribing information#

OTC Purpose Section

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

OTC Active Ingredient Section

OTC - ACTIVE INGREDIENT SECTION

OTC Active IngredientsOTC Active Ingredients

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

ARTWORK (SQZ TUBE)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

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
62932-246-412022-01-28C16284748780-1d6a99b39-cf16-a426-e053-dadaa90af4c2Suntegrity Natural Mineral Tinted Sunscreen Sport, Natural Tint

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-246-41SUNSCREEN85 g in 1 TUBEOINTMENT851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-246SUNSCREEN (ZINC OXIDE SUNSCREEN) OINTMENT [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20210101_b7c5f0b8-047c-5115-e053-2a95a90a1b4b.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
62932-24662932-246-41

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
ZINC OXIDESOI2LOH54ZACTIB
SHEA BUTTERK49155WL9YIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
MICAV8A1AW0880IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
FERRIC OXIDE RED1K09F3G675IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
WHITE WAX7G1J5DA97FIACT
SUNFLOWER OIL3W1JG795YIIACT
CASTOR OILD5340Y2I9GIACT
OLIVE OIL6UYK2W1W1EIACT
JOJOBA OIL724GKU717MIACT
FERRIC OXYHYDROXIDE87PZU03K0KIACT
.DELTA.-TOCOPHEROLJU84X1II0NIACT
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
.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
b7c5f0b8-047d-5115-e053-2a95a90a1b4bb7c5f0b8-047c-5115-e053-2a95a90a1b4b2020-12-31Exact identifier
spl id: b7c5f0b8-047d-5115-e053-2a95a90a1b4b
spl set id: b7c5f0b8-047c-5115-e053-2a95a90a1b4b

Reported adverse events (FAERS/openFDA)#

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