FDA.reportPublic FDA data

Sunbrellas Kids Sunblock SPF 45

Manufacturer
The Hain Celestial Group, Inc.
Effective date
2010-07-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:23

Label at a glance#

ProductSunbrellas Kids Sunblock SPF 45
Active ingredientHomosalate, Octocrylene, Octinoxate, Octisalate, Titanium Dioxide
Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS

Homosalate       10.0%

Octocrylene      10.0%

Ethylhexyl Methoxycinnamate    7.5%

Ethylhexyl Salicilate    5.0%

Titanium Dioxide    2.0%

INDICATIONS & USAGE SECTION

                             USES

  •     Helps prevent sunburns
  •     Higher SPF gives more sunburn protection
  •     Moderate sun protection product
  •     Apply sunscreen liberally to all exposed skin area 15 to 20 minutes before sun exposure
  •      Reapply as needed after towel drying, swimming or sweating
  •      Children under 6 months, ask doctor

WARNINGS SECTION

WARNINGS


For external use only. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask
a doctor if rash or irritation develops and lasts. Keep out of reach of children. If swallowed, get medical help or contact Poison Center right away.

USER SAFETY WARNINGS SECTION

OTHER INFORMATION

Sun Alert: Limiting Sun exposure, wearing protective clothing, and using sunscreen may reduce the risk of skin aging, skin cancer and other harmful effects of the sun.

OTC - QUESTIONS SECTION

QUESTIONS?

1-877-JASON-01

www.jason-natural.com

JASON NATURAL PRODUCTS

The Hain Celestial Group, Inc.

Melville, NY 11747

Made in U.S.A.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of tube labelimage of tube label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61995-0204-42019-10-21C16284748780-1956f9ecf-c3bd-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61995-0204-4Sunbrellas Kids Sunblock SPF 45113 g in 1 TUBECREAM1131

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61995-0204SUNBRELLAS KIDS SUNBLOCK SPF 45 (HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICILATE, TITANIUM DIOXIDE) CREAM [THE HAIN CELESTIAL GROUP, INC.]1Legacy NDC, 1 package rows20100730_ac77cd6d-de01-44eb-8f5d-cf172ec1b53b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HomosalateACTIVE INGREDIENTV06SV4M95S1
OctinoxateACTIVE INGREDIENT4Y5P7MUD511
OctisalateACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
HomosalateACTIVE MOIETYV06SV4M95S1
OctinoxateACTIVE MOIETY4Y5P7MUD511
OctisalateACTIVE MOIETY4X49Y0596W1
OctocryleneACTIVE MOIETY5A68WGF6WM1
Titanium DioxideACTIVE MOIETY15FIX9V2JP1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61995-020461995-0204-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
HomosalateV06SV4M95SACTIB
Octocrylene5A68WGF6WMACTIB
Octinoxate4Y5P7MUD51ACTIB
Octisalate4X49Y0596WACTIB
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
a4c30581-5f39-462a-905e-26f51673d47aac77cd6d-de01-44eb-8f5d-cf172ec1b53b2010-07-28WarningsExact identifier
spl id: a4c30581-5f39-462a-905e-26f51673d47a
spl set id: ac77cd6d-de01-44eb-8f5d-cf172ec1b53b

Reported adverse events (FAERS/openFDA)#

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