FDA.reportPublic FDA data

Cleanse Wise Antibacterial Hand Wipes

Manufacturer
Terraboost Media LLC
Effective date
2021-11-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:25:32

Label at a glance#

ProductCleanse Wise Antibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium chloride 0.13%

OTC - PURPOSE SECTION

Purpose

Antibacterial

INDICATIONS & USAGE SECTION

Uses

  • to decrease bacteria on the skin
  • recommended for repeated use

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • rub wipe thoroughly over all surfaces of both hands
  • allow to dry without wiping
  • supervise children under 6 years old
  • not recommended for infants
  • dispose of wipe in trash; do not flush

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Fragrance, C12-15 Alcohols, Chloroxylenol, Aloe Barbadensis Leaf Juice

SPL UNCLASSIFIED SECTION

Terraboost Media, LLC
3109 Grand Avenue #300

Miami, FL 33133

A product of Terraboost®

877-837-7210

www.tazzabrands.com

MADE IN USA WITH GLOBAL MATERIALS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fresh Scent

Cleanse Wise

ANTIBACTERIAL HAND WIPES

Kills 99.99% of germs

66% XXL LARGER WIPE OVER LEADING BRANDS

Hypoallergenic

Paraben Free

35 WET WIPES

WIPE SIZE 7" x 8" (17.78 cm x 20.32 cm)

CleanseWise 76370-0011CleanseWise 76370-0011

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
76370-001176370-0011-0

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
WATER059QF0KO0RIACT
CHLOROXYLENOL0F32U78V2QIACT
C12-15 ALCOHOLS2C8M6XLB5CIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT

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
df4cf31f-a146-6284-e053-2a95a90adbadc224ad0a-5d4d-09a2-e053-2995a90a000b2022-05-18WarningsExact identifier
spl set id: c224ad0a-5d4d-09a2-e053-2995a90a000b

Reported adverse events (FAERS/openFDA)#

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