FDA.reportPublic FDA data

Antibacterial Wet

Manufacturer
Xi'an Livingbond Nonwoven Products Corp., Ltd.
Effective date
2017-11-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:09:42

Label at a glance#

ProductAntibacterial Wet
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Indications and uses

For hand washing to decrease bacteria on the skin. May be used on face, arms and legs.

Dosage and administration

Tear open. Unfold the wipe. Clean hands or affected area and discard.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses:

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin. May be used on face, arms and legs.

Warnings:

WARNINGS SECTION

For external use only.

Keep out of reach of children,

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

except with adult supervision. Keep out of eyes. In case of contact, rinse with water. If irritation or rash develops, discontinue use. Consult doctor if irritation persists for more than 72 hours. If swallowed, seek medical attention or contact a Poison Control Center.

Directions:

DOSAGE & ADMINISTRATION SECTION

Tear open. Unfold the wipe. Clean hands or affected area and discard.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Glycerin, Lauryl Glucoside, DMDM, Hydantoin, Aloe Barbadensis Leaf Extract, Disodium EDTA, PEG 12, Dimethicone, Panthenol,  Chamomila Recutita (Matricaria) Extract, Lodopropynyl Butlycarbamae, Tocopheryl Acetate (Vitamin E), Allantoin.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50014-11050014-110-01, 50014-110-30, 50014-110-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
HYDANTOINI6208298TAIACT
ALOE VERA LEAFZY81Z83H0XIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
POLYETHYLENE GLYCOL 12000VM53EE110JIACT
DIMETHICONE92RU3N3Y1OIACT
PANTHENOLWV9CM0O67ZIACT
MATRICARIA CHAMOMILLAG0R4UBI2ZZIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ALLANTOIN344S277G0ZIACT
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
c2d9940a-ce7c-5fd0-e053-2a95a90a4bc809f0d5f2-b3d5-4d78-9cc7-51eafdd3df642021-05-21WarningsExact identifier
spl set id: 09f0d5f2-b3d5-4d78-9cc7-51eafdd3df64

Reported adverse events (FAERS/openFDA)#

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