FDA.reportPublic FDA data

Tinted Mineral Sunscreen, SPF 30 Medium Tint

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#

ProductTinted Mineral Sunscreen, SPF 30 Medium Tint
Active ingredientZINC OXIDE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - Active Section

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 Ingredients

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

Indications and Usage

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Warnings

WARNINGS SECTION

Warnings SectionWarnings Section

Artwork

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
62932-262-462023-01-30C16284748780-1f386c649-f1bb-0266-e053-dadaa90a7c1aOlita Inc., Tinted Mineral Sunscreen, SPF 30 (Medium Tint)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-262-46Tinted Mineral Sunscreen, SPF 30 Medium Tint89 g in 1 TUBEOINTMENT891

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-262TINTED MINERAL SUNSCREEN, SPF 30 MEDIUM TINT (SUNSCREEN) OINTMENT [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20220101_d4763e91-5daf-4a3c-e053-2a95a90af471.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
62932-26262932-262-46

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
.DELTA.-TOCOPHEROLJU84X1II0NIACT
WHITE WAX7G1J5DA97FIACT
OLIVE OIL6UYK2W1W1EIACT
FERRIC OXYHYDROXIDE87PZU03K0KIACT
JOJOBA OIL724GKU717MIACT
SHEA BUTTERK49155WL9YIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
FERRIC OXIDE RED1K09F3G675IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
.BETA.-TOCOPHEROL9U6A490501IACT
SUNFLOWER OIL3W1JG795YIIACT
MICAV8A1AW0880IACT
ZINC OXIDESOI2LOH54ZACTIB
CASTOR OILD5340Y2I9GIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT

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
d4763e91-5dae-4a3c-e053-2a95a90af471d4763e91-5daf-4a3c-e053-2a95a90af4712021-12-31WarningsExact identifier
spl id: d4763e91-5dae-4a3c-e053-2a95a90af471
spl set id: d4763e91-5daf-4a3c-e053-2a95a90af471

Reported adverse events (FAERS/openFDA)#

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