FDA.reportPublic FDA data

SUNSCREEN

Manufacturer
Private Label Select Ltd CO
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:46:18

Label at a glance#

ProductSUNSCREEN
Active ingredientZINC OXIDE
Label structure2 sections

Label contents#

Full prescribing information#

made of Sunscreen SPF30 Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

made of Sunscreen Lotion SPF30 Tubemade of Sunscreen Lotion SPF30 Tube

made of Sunscreen Lotion SPF30 Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

made of Sunscreen SPF30 Boxmade of Sunscreen SPF30 Box

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-182-212023-07-28C16284748780-19d75b9d1-144f-f424-e053-dadaa90a57cemade of Sunscreen SPF30
62932-182-212022-01-04C16284748780-19d75b9d1-144f-f424-e053-dadaa90a57cemade of Sunscreen SPF30
62932-182-212020-01-31C16284748780-19d75b9d1-144f-f424-e053-dadaa90a57cemade of Sunscreen SPF30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-182-21SUNSCREEN113 g in 1 TUBEOINTMENT1132

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-182SUNSCREEN (ZINC OXIDE SUNSCREEN) OINTMENT [PRIVATE LABEL SELECT LTD CO]2Legacy NDC, 1 package rows20220105_7b5de2ca-99c9-60e6-e053-2991aa0ab0b5.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
62932-18262932-182-21

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
ZINC OXIDESOI2LOH54ZACTIB
HELIANTHUS ANNUUS SEED WAX42DG15CHXVIACT
COCONUT OILQ9L0O73W7LIACT
YELLOW WAX2ZA36H0S2VIACT
THEOBROMA GRANDIFLORUM SEED BUTTERI711F13FXMIACT
VANILLAQ74T35078HIACT
TOCOPHEROLR0ZB2556P8IACT
ARGAN OIL4V59G5UW9XIACT
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
d4c94129-eaec-b168-e053-2995a90a76837b5de2ca-99c9-60e6-e053-2991aa0ab0b52022-01-04Exact identifier
spl id: d4c94129-eaec-b168-e053-2995a90a7683
spl set id: 7b5de2ca-99c9-60e6-e053-2991aa0ab0b5

Reported adverse events (FAERS/openFDA)#

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