FDA.reportPublic FDA data

Antibacterial Wet Wipes

Manufacturer
HANGZHOU SUNKING NOWOVENS CO., LTD.
Effective date
2018-11-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:45:00

Label at a glance#

ProductAntibacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Indications and uses

For hand washing to decrease bacteria on skin

Dosage and administration

Thoroughly wipe hands or face with wipe. Discard in trash receptacle; Do not flush. Be sure to reseal label complete to retain moisture.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on skin

Warnings

WARNINGS SECTION

  • For external use only

Do not use

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients

When using this products

OTC - WHEN USING SECTION

  • do not get into eyes. If contact occurs, rinse thoroughly with water
  • Discontinue use if irritation or redness develops if condition persists for more than 72 hours consult a physician

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions For Use

DOSAGE & ADMINISTRATION SECTION

Thoroughly wipe hands or face with wipe. Discard in trash receptacle; Do not flush. Be sure to reseal label complete to retain moisture.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Disodium ETDA, Chloromethylisothiazolinone & Methylisothiazolinone, Potassium Sorbate, Quaternium-15, Aloe
Barbadensis Leaf Juice, Dissodium Cocoamphodjacetate, Tocophery Acetate, Polysorbate-20, Citric Acid, Fragrance

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43935-00043935-000-30, 43935-000-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
EDETATE DISODIUM7FLD91C86KIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
QUATERNIUM-15E40U03LEM0IACT
ALOE VERA LEAFZY81Z83H0XIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
POLYSORBATE 207T1F30V5YHIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
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
7be779de-11f7-cccf-e053-2991aa0a77ac15ff4dce-7a5e-434b-a2fc-d9b208008e402018-11-30WarningsExact identifier
spl id: 7be779de-11f7-cccf-e053-2991aa0a77ac
spl set id: 15ff4dce-7a5e-434b-a2fc-d9b208008e40

Reported adverse events (FAERS/openFDA)#

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