FDA.reportPublic FDA data

SUNSCREEN

Manufacturer
Private Label Select Ltd CO
Effective date
2020-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:45

Label at a glance#

ProductSUNSCREEN
Active ingredientZINC OXIDE
Label structure9 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 put of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC Keep put of reach of childrenOTC Keep put of reach of children

OTC Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

OTC Active IngredientOTC Active Ingredient

OTC Purpose

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

Label/Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Display Case

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Display CartonDisplay Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-217-382022-01-28C16284748780-1d6a99b39-bc05-a426-e053-dadaa90af4c2Vertra Lip Balm Moisturizing Sunscreen, SPF 15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-217-38SUNSCREEN4.25 g in 1 CONTAINERSTICK4.251
62932-217-38SUNSCREEN12 in 1 CARTONSTICK121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-217SUNSCREEN (ZINC OXIDE SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 2 package rows20200402_a2403cdf-838f-e496-e053-2a95a90ae60a.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62932-21762932-217-38

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
SHEA BUTTERK49155WL9YIACT
TAMANU OILJT3LVK84A1IACT
COCOA BUTTER512OYT1CRRIACT
COCONUT OILQ9L0O73W7LIACT
JOJOBA OIL724GKU717MIACT
ZINC OXIDESOI2LOH54ZACTIB
WHITE WAX7G1J5DA97FIACT
SUNFLOWER OIL3W1JG795YIIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
TOCOPHEROLR0ZB2556P8IACT
RASPBERRY SEED OIL9S8867952AIACT

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
a2403cdf-8390-e496-e053-2a95a90ae60aa2403cdf-838f-e496-e053-2a95a90ae60a2020-04-01WarningsExact identifier
spl id: a2403cdf-8390-e496-e053-2a95a90ae60a
spl set id: a2403cdf-838f-e496-e053-2a95a90ae60a

Reported adverse events (FAERS/openFDA)#

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