FDA.reportPublic FDA data

Antibacterial Wet 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 Wet 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 out rinsing. Discard after single use

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antiseptic

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 out rinsing.
  • Discard after single use

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

Aqua, Glycerin, Phenoxyethanol, Benzoic Acid, Polysorbate 20, Aloe Barbadensis Leaf Juice, Sodium Citrate

Package Labeling:15 count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79021-00379021-003-15

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BENZOIC ACID8SKN0B0MIMIACT
POLYSORBATE 207T1F30V5YHIACT
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM CITRATE1Q73Q2JULRIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
08be3a9f-6760-d317-e063-6394a90a8fb1af487a42-0c8d-0090-e053-2a95a90afb502024-01-26WarningsExact identifier
spl set id: af487a42-0c8d-0090-e053-2a95a90afb50

Reported adverse events (FAERS/openFDA)#

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