FDA.reportPublic FDA data

Antibacterial Wet Wipes

Manufacturer
Positive Promotions Inc.
Effective date
2021-11-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:25:43

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

Take wipe and rub thoroughly over the surface of both hands, then rub hands briskly to dry. Dispose after single use. Do not flush.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

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.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact with eyes, flush thoroughly with water.

Stop use & ask a doctor

OTC - STOP USE SECTION

if irritation and redness develops and persist for more than 72 hours.

Keep out of reach from children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Take wipe and rub thoroughly over the surface of both hands, then rub hands briskly to dry.
  • Dispose after single use.
  • Do not flush.

Other information

SPL UNCLASSIFIED SECTION

  • Keep away from sunlight. Store at room temperature 20°-25° Celsius (68°-77° Fahrenheit)
  • May discolor certain fabrics.

Package Labeling:80 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
79021-00579021-005-80

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
08be3e93-6374-6e37-e063-6294a90a2a6cb25b91e9-497a-1f80-e053-2a95a90af0792023-10-27WarningsExact identifier
spl set id: b25b91e9-497a-1f80-e053-2a95a90af079

Reported adverse events (FAERS/openFDA)#

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