Antibacterial Wipes

Manufacturer
Positive Promotions Inc.
Effective date
2021-11-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:25:42

Label at a glance#

ProductAntibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

For hand-washing to decrease bacteria on skin

Dosage and administration

Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation. Thoroughly wipe hands, allow to dry without rinsing. Discard after single use Use within a month of opening

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • For hand-washing to decrease bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from heat and flame.
For External use only.

Do not use

OTC - DO NOT USE SECTION

in eyes. In case of contact, rinse thoroughly with water.

Stop use & ask doctor

OTC - STOP USE SECTION

if rash/redness or irritation appears/develops and persist for more than 72 hours.

Keep out of reach from children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

Directions

DOSAGE & ADMINISTRATION SECTION

  • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation.
  • Thoroughly wipe hands, allow to dry without rinsing.
  • Discard after single use
  • Use within a month of opening

Other information

SPL UNCLASSIFIED SECTION

  • Do not flush down toilet.
  • Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit)
  • May discolor certain fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Proylene Glycol, Aqua, Kathon, Tocopherol, Fragrance

Package Labeling:60 count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79021-00479021-004-60

Ingredients#

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

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

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
08bf1a51-d8de-edb2-e063-6294a90aedd4af489317-86eb-9921-e053-2a95a90a4e6e2023-10-27WarningsExact identifier
spl set id: af489317-86eb-9921-e053-2a95a90a4e6e

Reported adverse events (FAERS/openFDA)#

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