FDA.reportPublic FDA data

Antibacterial Wet Wipes

Manufacturer
Zhejiang Easyclean Daily Chemical Co., Ltd.
Effective date
2022-03-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:05:39

Label at a glance#

ProductAntibacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

●Thoroughly wipe hands as desired. ●Allow to dry without wiping. ●Discard wipe in trash after use. Do Not Flush.

Label contents#

Full prescribing information#

Active Ingredient Section

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

USE

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warning

WARNINGS SECTION

●For external use only
●Keep out of reach of children, except with adult supervision
●Keep out of eyes. In case of eye contact, rinse with water
●If irritation develops, stop using & consult a doctor if it persists for more than 72 hours.
●If swallowed, seek medical attention or contact a Poison Control Center

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach from children except under adult supervision.

Directions

DOSAGE & ADMINISTRATION SECTION

●Thoroughly wipe hands as desired.
●Allow to dry without wiping.
●Discard wipe in trash after use. Do Not Flush.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73760-004-012022-03-19C16284748780-1d6a99b39-8f76-a426-e053-dadaa90af4c273760-004 Antibacterial Wet Wipes 0.13%Benzalkonium Chloride
73760-004-012022-01-28C16284748780-1d6a99b39-8f76-a426-e053-dadaa90af4c273760-004 Antibacterial Wet Wipes 0.13%Benzalkonium Chloride

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
73760-00473760-004-01

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
PHENOXYETHANOLHIE492ZZ3TIACT
BENZOIC ACID8SKN0B0MIMIACT
POLYSORBATE 207T1F30V5YHIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
SODIUM CITRATE1Q73Q2JULRIACT
ALOE VERA LEAFZY81Z83H0XIACT
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
da91c464-4199-3a59-e053-2a95a90a2dc4a8f39dde-bb3f-e519-e053-2a95a90a65682022-03-19WarningsExact identifier
spl id: da91c464-4199-3a59-e053-2a95a90a2dc4
spl set id: a8f39dde-bb3f-e519-e053-2a95a90a6568

Reported adverse events (FAERS/openFDA)#

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