FDA.reportPublic FDA data

Alba Sunblock Natural FF SPF 30

Manufacturer
The Hain Celestial Group, Inc.
Effective date
2010-07-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:06

Label at a glance#

ProductAlba Sunblock Natural FF SPF 30
Active ingredientHomosalate, Octocrylene, Octisalate, Titanium Dioxide
Label structure5 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS

Homosalate       7.5%

Octocrylene      7.5%

Ethylhexyl Salicilate    5.0%

Titanium Dioxide    2.0%

INDICATIONS & USAGE SECTION

                               USES

  •     Helps prevent sunburns
  •     Higher SPF gives more sunburn protection
  •     Apply liberally as needed 15 to 20 minutes before sun exposure
  •      Reapply as needed or after swimming, perspiring or towel drying
  •      Children under 6 months of age: 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.

OTC - QUESTIONS SECTION

QUESTIONS?

Call (888) 659-7730 or visit www.AlbaBotanica.com

100% Vegetarian Ingredients

No Animal Testing

Alba Botanica

The Hain Celestial Group, Inc.

Melville, NY 11747

Made in the 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
61995-2391-42019-10-21C16284748780-1956f9ecf-df7a-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61995-2391-4Alba Sunblock Natural FF SPF 30113 g in 1 TUBECREAM1131

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61995-2391ALBA SUNBLOCK NATURAL FF SPF 30 (HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICILATE, TITANIUM DIOXIDE) CREAM [THE HAIN CELESTIAL GROUP, INC.]1Legacy NDC, 1 package rows20100708_91b1cee5-b0b4-4fed-befb-a28c7b1818fc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HomosalateACTIVE INGREDIENTV06SV4M95S1
OctisalateACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
HomosalateACTIVE MOIETYV06SV4M95S1
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 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61995-239161995-2391-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
HomosalateV06SV4M95SACTIB
Octocrylene5A68WGF6WMACTIB
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
5966a1a7-67e7-4097-87a9-9bb64263254f91b1cee5-b0b4-4fed-befb-a28c7b1818fc2010-07-07WarningsExact identifier
spl id: 5966a1a7-67e7-4097-87a9-9bb64263254f
spl set id: 91b1cee5-b0b4-4fed-befb-a28c7b1818fc

Reported adverse events (FAERS/openFDA)#

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