Medi-First Plus Antiseptic 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: Medi-First Plus Antiseptic Wipes
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Unifirst First Aid Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 5743634b-f329-5fec-e053-2991aa0a751d
SPL ID: 3e4c7566-32b5-4d29-e063-6394a90a93b1
Version: 9
Effective date: 2025-09-08
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:41

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Medi-First Antiseptic Wipes	openfda.brand_name
brand name		Medi-First Plus Antiseptic Wipes	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Unifirst First Aid Corporation	openfda.manufacturer_name
ndc	package	47682-030-71	openfda.package_ndc
ndc	package	47682-212-71	openfda.package_ndc
ndc	package	47682-212-12	openfda.package_ndc
ndc	package	47682-212-33	openfda.package_ndc
ndc	product	47682-030	openfda.product_ndc
ndc	product	47682-212	openfda.product_ndc
ndc11	package	47682003071	derived:openfda.package_ndc
ndc11	package	47682021233	derived:openfda.package_ndc
ndc11	package	47682021271	derived:openfda.package_ndc
ndc11	package	47682021212	derived:openfda.package_ndc
rxcui		1043307	openfda.rxcui
spl id		3e4c7566-32b5-4d29-e063-6394a90a93b1	id
spl set id		5743634b-f329-5fec-e053-2991aa0a751d	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

Warnings Do not use in the eyes or over large areas of the body in case of deep or puncture woulds, animal bite or serious burns, consult a doctor longer than 1 week unless directed by a doctor Stop use and ask a doctor if 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.