FDA.reportPublic FDA data

The Green Beaver Company SPF 40 Kids Sunscreen

Manufacturer
The Green Beaver Company | Regulatory Matters Consulting
Effective date
2021-01-11
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:36:47

Label at a glance#

ProductThe Green Beaver Company SPF 40 Adult Sunscreen
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredientActive ingredient

OTC - PURPOSE SECTION

PurposePurpose

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reachKeep out of reach

INDICATIONS & USAGE SECTION

UsesUses

DOSAGE & ADMINISTRATION SECTION

DirectionsDirections

WARNINGS SECTION

WarningsWarnings

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sunscreen SPF 40Sunscreen SPF 40

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76098-003-012023-01-30C16284748780-1f386c64a-04c6-0266-e053-dadaa90a7c1aThe Green Beaver Adults Sunscreen SPF 40

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76098-003-01The Green Beaver Company SPF 40 Adult Sunscreen94 g in 1 TUBELOTION946

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76098-003THE GREEN BEAVER COMPANY SPF 40 ADULT SUNSCREEN (SUNSCREEN LOTION) LOTION [THE GREEN BEAVER COMPANY]6Legacy NDC, 1 package rows20210112_63a49b3f-de86-5397-e053-2991aa0a7a06.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76098-00376098-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
CEROTIC ACIDD42CQN6P36IACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
ALUMINUM OXIDELMI26O6933IACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
TRIHYDROXYSTEARIN06YD7896S3IACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
SODIUM BETA-SITOSTERYL SULFATEI289C8TPSVIACT
SQUALENE7QWM220FJHIACT
LECITHIN, SUNFLOWER834K0WOS5GIACT
KARUM SEED OIL62160PU6FJIACT
HELIANTHUS ANNUUS SEED WAX42DG15CHXVIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDEFJ1H6M2JG9IACT
RUBUS IDAEUS FRUIT VOLATILE OIL276X2YNL0KIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
WATER059QF0KO0RIACT
ISOSTEARIC ACIDX33R8U0062IACT
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
b8a64f9e-1a47-191f-e053-2a95a90ae62863a49b3f-de86-5397-e053-2991aa0a7a062021-01-11WarningsExact identifier
spl id: b8a64f9e-1a47-191f-e053-2a95a90ae628
spl set id: 63a49b3f-de86-5397-e053-2991aa0a7a06

Reported adverse events (FAERS/openFDA)#

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