FDA.reportPublic FDA data

Summer Lotion SPF 30 Natural Sunscreen Lotion

Manufacturer
Private Label Select Ltd CO
Effective date
2019-12-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:02:27

Label at a glance#

ProductSUNSCREEN
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

DosageDosage

Warnings

WARNINGS SECTION

WarningsWarnings

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

Indications & Usage

INDICATIONS & USAGE SECTION

Indications & UsageIndications & Usage

OTC Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC Keep Out of ReachOTC Keep Out of Reach

OTC Purpose Section

OTC - PURPOSE SECTION

PurposePurpose

OTC Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Squeeze Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

Unit Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Unit CartonUnit Carton

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
62932-205-212021-01-29C16284748780-1ba0f9c33-357f-a910-e053-dadaa90a0b85Summer Lotion SPF 30 Natural Sunscreen Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-205-21SUNSCREEN1 in 1 CARTONOINTMENT11
62932-205-21SUNSCREEN113 g in 1 TUBEOINTMENT1131

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-205SUNSCREEN (ZINC OXIDE SUNSREEN) OINTMENT [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 2 package rows20191229_9acc4979-080b-290b-e053-2995a90ad542.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
62932-20562932-205-21

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
CASTOR OILD5340Y2I9GIACT
JOJOBA OIL724GKU717MIACT
TOCOPHEROLR0ZB2556P8IACT
ZINC OXIDESOI2LOH54ZACTIB
COCONUT OILQ9L0O73W7LIACT
OLIVE OIL6UYK2W1W1EIACT
SHEA BUTTERK49155WL9YIACT
WHITE WAX7G1J5DA97FIACT
SUNFLOWER OIL3W1JG795YIIACT

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
9acc4ef9-64cd-2fb4-e053-2995a90aa21a9acc4979-080b-290b-e053-2995a90ad5422019-12-28WarningsExact identifier
spl id: 9acc4ef9-64cd-2fb4-e053-2995a90aa21a
spl set id: 9acc4979-080b-290b-e053-2995a90ad542

Reported adverse events (FAERS/openFDA)#

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