antiseptic towelette 01

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: antiseptic towelette 01
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Cosmuses Cosmetics (Ningbo) Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: e9f2a1f1-ceb6-2f20-e053-2a95a90a18db
SPL ID: 286c802e-e0fd-9b20-e063-6394a90a504a
Version: 2
Effective date: 2024-12-04
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:33

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 · 35 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		antiseptic towelette 01	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Cosmuses Cosmetics (Ningbo) Co., Ltd.	openfda.manufacturer_name
ndc	package	82953-004-11	openfda.package_ndc
ndc	package	82953-004-08	openfda.package_ndc
ndc	package	82953-004-07	openfda.package_ndc
ndc	package	82953-004-09	openfda.package_ndc
ndc	package	82953-004-13	openfda.package_ndc
ndc	package	82953-004-03	openfda.package_ndc
ndc	package	82953-004-01	openfda.package_ndc
ndc	package	82953-004-05	openfda.package_ndc
ndc	package	82953-004-12	openfda.package_ndc
ndc	package	82953-004-04	openfda.package_ndc
ndc	package	82953-004-02	openfda.package_ndc
ndc	package	82953-004-10	openfda.package_ndc
ndc	package	82953-004-06	openfda.package_ndc
ndc	product	82953-004	openfda.product_ndc
ndc11	package	82953000410	derived:openfda.package_ndc
ndc11	package	82953000411	derived:openfda.package_ndc
ndc11	package	82953000405	derived:openfda.package_ndc
ndc11	package	82953000401	derived:openfda.package_ndc
ndc11	package	82953000407	derived:openfda.package_ndc
ndc11	package	82953000404	derived:openfda.package_ndc
ndc11	package	82953000412	derived:openfda.package_ndc
ndc11	package	82953000406	derived:openfda.package_ndc
ndc11	package	82953000408	derived:openfda.package_ndc
ndc11	package	82953000402	derived:openfda.package_ndc
ndc11	package	82953000413	derived:openfda.package_ndc
ndc11	package	82953000403	derived:openfda.package_ndc
ndc11	package	82953000409	derived:openfda.package_ndc
rxcui		1038558	openfda.rxcui
spl id		286c802e-e0fd-9b20-e063-6394a90a504a	id
spl set id		e9f2a1f1-ceb6-2f20-e053-2a95a90a18db	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 For external use only. Do not use in the eyes. If this happens, rinse thoroughly with water. Stop use and ask a doctor if irritation or redness develop and persists for more than 72 hours. Keep out of reach of children if swallowed, get medical help or contact a poison control center right away.

Reported adverse events (FAERS/openFDA)#

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