Antibacterial Wet wipes

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Antibacterial Wet wipes
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Zhejiang Easyclean Daily Chemical Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: a1cb6ac9-95f5-3ef1-e053-2a95a90abcdf
SPL ID: 4a98ca2f-0213-be6c-e063-6294a90a5714
Version: 8
Effective date: 2026-02-11
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:29:16

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Antibacterial Wet wipes	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Zhejiang Easyclean Daily Chemical Co., Ltd.	openfda.manufacturer_name
ndc	package	73760-001-04	openfda.package_ndc
ndc	package	73760-001-09	openfda.package_ndc
ndc	package	73760-001-02	openfda.package_ndc
ndc	package	73760-001-03	openfda.package_ndc
ndc	package	73760-001-08	openfda.package_ndc
ndc	package	73760-001-07	openfda.package_ndc
ndc	package	73760-001-05	openfda.package_ndc
ndc	package	73760-001-06	openfda.package_ndc
ndc	package	73760-001-01	openfda.package_ndc
ndc	product	73760-001	openfda.product_ndc
ndc11	package	73760000108	derived:openfda.package_ndc
ndc11	package	73760000103	derived:openfda.package_ndc
ndc11	package	73760000101	derived:openfda.package_ndc
ndc11	package	73760000105	derived:openfda.package_ndc
ndc11	package	73760000102	derived:openfda.package_ndc
ndc11	package	73760000104	derived:openfda.package_ndc
ndc11	package	73760000109	derived:openfda.package_ndc
ndc11	package	73760000106	derived:openfda.package_ndc
ndc11	package	73760000107	derived:openfda.package_ndc
rxcui		1038558	openfda.rxcui
spl id		4a98ca2f-0213-be6c-e063-6294a90a5714	id
spl set id		a1cb6ac9-95f5-3ef1-e053-2a95a90abcdf	set_id
unii		F5UM2KM3W7	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warning Flammable. Keep away from heat and flame. For External use only. Do not use in eyes. In case of contact, rinse thoroughly with water. Stop use & ask doctor if rash/redness or irritation appears/develops and persist for more than 72 hours. Keep out of reach from children except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

Reported adverse events (FAERS/openFDA)#

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