FDA.reportPublic FDA data

Antibacterial wipes

Manufacturer
Kangna (Zhejiang) Medical Supplies Co., Ltd.
Effective date
2022-01-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:16:46

Label at a glance#

ProductAntibacterial wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

●Gently pull back resealable label, remove and use wipe as required. ， Reseal back after use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.3%

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.
●Recommended for repeated use.
●Dries in seconds.

Warning

WARNINGS SECTION

●For external use only.
●Do not use in or contact the eyes.
" Stop use and ask a doctor if too much skin irritation or
sensitivity develops or increases.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

●Keep out of reach of children. If swallowed, get medical
help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

●Gently pull back resealable label, remove and use wipe
as required.
， Reseal back after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, DMDM Hydantoin, Ethylparaben,
Methylparaben, Polysorbate 20, Fragrance, Disodium EDTA,
Sodium Citrate, Cetylpyridinium Chloride.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75109-50475109-504-01, 75109-504-02, 75109-504-03, 75109-504-04, 75109-504-05, 75109-504-06, 75109-504-07, 75109-504-08, 75109-504-09, 75109-504-10, 75109-504-11, 75109-504-12

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
NameUNIIKind
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
WATER059QF0KO0RIACT
DMDM HYDANTOINBYR0546TOWIACT
POLYSORBATE 207T1F30V5YHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLPARABEN14255EXE39IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
METHYLPARABENA2I8C7HI9TIACT
SODIUM CITRATE1Q73Q2JULRIACT

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
d5873b92-2a55-cb36-e053-2995a90aef93a8a1846f-1f3e-cdcb-e053-2a95a90ae6472022-01-14WarningsExact identifier
spl id: d5873b92-2a55-cb36-e053-2995a90aef93
spl set id: a8a1846f-1f3e-cdcb-e053-2a95a90ae647

Reported adverse events (FAERS/openFDA)#

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