FDA.reportPublic FDA data

SpongeBob HandSanitizer

Manufacturer
Taste Beauty LLC
Effective date
2020-07-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:19:08

Label at a glance#

ProductSpongeBob HandSanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire and flames.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On open skin wounds

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes, ears and mouth.
  • In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Irritation and redness develop.

These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

OTHER SAFETY INFORMATION

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C(104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Fragrance/Parfum, PEG-40 Hydrogenated Castor Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Hydroxide, Denatonium Benzoate, D&C Red No. 4 (Cl 14700)

Principal Display Panel – 30 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand
Sanitizer

pinapple scented

1 FL OZ/30 mL

Principal Display Panel – 30 mL Bottle Label
Principal Display Panel – 30 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74825-9025-12022-02-01C16284748780-1d6a99b39-9266-a426-e053-dadaa90af4c2Drug Facts
74825-9025-12022-01-28C16284748780-1d6a99b39-9266-a426-e053-dadaa90af4c2Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74825-902574825-9025-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
Water059QF0KO0RIACT
Polyethylene Glycol 2000HAF0412YITIACT
Hydrogenated Castor OilZF94AP8MEYIACT
Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked)59TL3WG5COIACT
Sodium Hydroxide55X04QC32IIACT
Denatonium Benzoate4YK5Z54AT2IACT
FD&C Red No. 4X3W0AM1JLXIACT

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
fb74ac05-6fd2-467d-90f6-d72f957f2af3d1b08aeb-5df3-4232-adfc-fc6d75f9ba512022-02-01WarningsExact identifier
spl set id: d1b08aeb-5df3-4232-adfc-fc6d75f9ba51

Reported adverse events (FAERS/openFDA)#

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