Antibacterial Eco Wipes

Manufacturer: Kangna (Zhejiang) Medical Supplies Co., Ltd.
Effective date: 2023-01-12
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 21:40:32

Label at a glance#

ProductAntibacterial Eco Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Dosage and administration

Gently pull back resealable label, remove and use wipes as required. Reseal back after use to retain moisture.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

●For hand sanitizing to decrease bacteria on the skin.
●Apply topically to the skin to help prevent cross contamination.
●Not recommended for repeated use.
●Dries in seconds.

Warning

WARNINGS SECTION

For external use only.
When using this product keep out of eyes, ears, and mouth. In case of eye contact, flush thoroughly with water.
Stop use and ask doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Posion Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Gently pull back resealable label, remove and use wipes as required.
Reseal back after use to retain moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, DMDM Hydantoin, Ethylparaben, Methylparaben, Polysorbate 20, Fragrance,
Disodium EDTA, Sodium Citrate, Aloe Barbadensis Leaf Juice.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Antibacterial Eco Wipes
Benzalkonium Chloride
ALOE VERA LEAF
WATER
DMDM HYDANTOIN
POLYSORBATE 20
PHENOXYETHANOL
ETHYLPARABEN
BENZALKONIUM
EDETATE DISODIUM ANHYDROUS
METHYLPARABEN
SODIUM CITRATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75109-522	75109-522-04, 75109-522-05, 75109-522-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
ETHYLPARABEN	14255EXE39	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
EDETATE DISODIUM ANHYDROUS	8NLQ36F6MM	IACT
METHYLPARABEN	A2I8C7HI9T	IACT
SODIUM CITRATE	1Q73Q2JULR	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f20e3bb7-0c35-aca0-e053-2a95a90a423b			bd4e3d04-8720-4b31-e053-2995a90a9aa7	2023-01-12	Warnings	Exact identifier spl id: f20e3bb7-0c35-aca0-e053-2a95a90a423b spl set id: bd4e3d04-8720-4b31-e053-2995a90a9aa7

Reported adverse events (FAERS/openFDA)#

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