FDA.reportPublic FDA data

Spongebob Squarepants Antibacterial Wipes

Manufacturer
Taste Beauty LLC | Zhejiang iColor Biotech Co., Ltd
Effective date
2020-11-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:58:08

Label at a glance#

ProductSpongebob Squarepants Antibacterial Wipes
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Unfold towlette, wipe hands, rub hands until dry. To dispense, peel back front label, remove wipe. To dispose, place in waste basket after use. Do not flush.

Label contents#

Full prescribing information#

Active ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Use:

INDICATIONS & USAGE SECTION

Single use hand wipes to clean & reduce bacteria

Warnings:

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire and flames.

Do not use

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

OTC - WHEN USING SECTION

When using this product

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

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Irritation or rash occurs.

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

  • Unfold towlette, wipe hands, rub hands until dry.
  • To dispense, peel back front label, remove wipe.
  • To dispose, place in waste basket after use.
  • Do not flush.

Other information

OTHER SAFETY INFORMATION

  • Store between 15-30°C (59-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Aloe Barbadensis Leaf Extract, Fragrance.

Principal Display Panel – 20 Count Bag Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

nickelodeon

SPONGEBOB
SQUAREPANTS

ANTIBACTERIAL
WIPES

Kills 99.9% of Germs

Contains 75% Alcohol

Ocean Breeze Scent

20 COUNT

OPEN

5.9 in x 7 in (150mm x 180mm) wipes

Principal Display Panel – 20 Count Bag Label
Principal Display Panel – 20 Count Bag Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74825-9125-12022-02-01C16284748780-1d6a99b39-b413-a426-e053-dadaa90af4c2Drug Facts
74825-9125-12022-01-28C16284748780-1d6a99b39-b413-a426-e053-dadaa90af4c2Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74825-912574825-9125-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
Water059QF0KO0RIACT
Aloe Vera Flower575DY8C1ERIACT

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
3b840cfd-3c1b-4e53-9a89-2741e4feb2fa0bd4d902-fe0d-4a9c-b901-a6e22d9ba4922022-02-01WarningsExact identifier
spl set id: 0bd4d902-fe0d-4a9c-b901-a6e22d9ba492

Reported adverse events (FAERS/openFDA)#

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