Antibacterial Wet Wipes

Manufacturer
Zhejiang Ayan Biotech Co.,Ltd.
Effective date
2023-11-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:59:14

Label at a glance#

ProductAntibacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 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

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 without 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

Water(aqua), Propylene Glycol, Tocopherol, Kathon

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN5
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD5
1038558benzalkonium chloride 0.13 % Topical ClothSY5
1038558benzalkonium chloride 0.13 % Topical SwabSY5
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY5
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY5
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70412-500-10Antibacterial Wet Wipes10 in 1 BOXCLOTH105
70412-500-10Antibacterial Wet Wipes5 g in 1 PATCHCLOTH55
70412-500-50Antibacterial Wet Wipes3.6 g in 1 PATCHCLOTH3.65
70412-500-50Antibacterial Wet Wipes50 in 1 BOXCLOTH505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70412-500ANTIBACTERIAL WET WIPES (BENZALKONIUM CHLORIDE) CLOTH [ZHEJIANG AYAN BIOTECH CO.,LTD.]5Current NDC, Legacy NDC, 4 package rows20231108_21b48552-e624-455c-938f-8151e58d80e0.zip

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
70412-50070412-500-10, 70412-500-50

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 · Source PDF

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
Antibacterial Wet WipesBENZALKONIUM CHLORIDEZhejiang Ayan Biotech Co.,Ltd.21b48552-e624-455c-938f-8151e58d80e02023-11-06WarningsExact identifier
ndc (package): 70412-500-10
ndc (package): 70412-500-50
ndc (product): 70412-500
ndc11 (package): 70412050010
ndc11 (package): 70412050050
spl id: 09874009-51dc-ac30-e063-6394a90ae5b4
spl set id: 21b48552-e624-455c-938f-8151e58d80e0

Reported adverse events (FAERS/openFDA)#

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