FDA.reportPublic FDA data

SUNSCREEN

Manufacturer
Private Label Select Ltd CO
Effective date
2022-05-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:49:33

Label at a glance#

ProductSUNSCREEN
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient Section

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

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

Purpose Section

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

Warnings Section

WarningsWarnings

Label Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

Unit Carton Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Artwork UCArtwork UC

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-267-382023-07-28C16284748780-10191ceaa-6ae3-198a-e063-dbdaa90aec3eSoleil Toujours, Summer Camp Mineral BFF Lip Jam, SPF 15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-267-38SUNSCREEN1 in 1 CARTONSTICK11
62932-267-38SUNSCREEN4.2 g in 1 CONTAINERSTICK4.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-267SUNSCREEN (ZINC OXIDE LIP BALM) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 2 package rows20220512_de4a0535-6233-1a40-e053-2a95a90a2ca5.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
62932-26762932-267-38

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
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
SHEA BUTTERK49155WL9YIACT
COCOA BUTTER512OYT1CRRIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
ZINC OXIDESOI2LOH54ZACTIB
WHITE WAX7G1J5DA97FIACT
SUNFLOWER OIL3W1JG795YIIACT
RASPBERRY SEED OIL9S8867952AIACT
.DELTA.-TOCOPHEROLJU84X1II0NIACT
TAMANU OILJT3LVK84A1IACT
POLYHYDROXYSTEARIC ACID STEARATE8KQ7I65XZEIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
JOJOBA OIL724GKU717MIACT
.BETA.-TOCOPHEROL9U6A490501IACT
COCONUT OILQ9L0O73W7LIACT

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
de4a0535-6234-1a40-e053-2a95a90a2ca5de4a0535-6233-1a40-e053-2a95a90a2ca52022-05-05WarningsExact identifier
spl id: de4a0535-6234-1a40-e053-2a95a90a2ca5
spl set id: de4a0535-6233-1a40-e053-2a95a90a2ca5

Reported adverse events (FAERS/openFDA)#

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