MediChoice BZK Antiseptic

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
MediChoice BZK Antiseptic
Generic name
BENZALKONIUM CHLORIDE
Manufacturer
O&M HALYARD, INC.
Product type
HUMAN OTC DRUG
SPL set ID
82a7710d-a9fa-4f68-8322-046a765ae929
SPL ID
40b21f22-24de-fe9f-e063-6394a90a7e66
Version
9
Effective date
2025-10-08
Source export date
2026-11-06
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/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:01:27
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use on mucous membranes or broken or irritated skin. Do not use Do not use in the eyes or apply over large areas of the body. longer than 1 week unless directed by a doctor. no infants. Consult a doctor in case of deep or punture wounds, animal bites, or serious burns. Stop use and consult a doctor If the condition persists or gets worse. 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.