Green Guard 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: Green Guard Antiseptic Wipes
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Uniforst First Aid Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 5744f9a2-35c6-37df-e053-2991aa0a1ca9
SPL ID: 3e4cb995-be1e-a159-e063-6294a90ae6e3
Version: 10
Effective date: 2025-09-08
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:43

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		Green Guard Antiseptic Wipes	openfda.brand_name
brand name		Green Guard Antideptic Wipes	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Uniforst First Aid Corporation	openfda.manufacturer_name
ndc	package	47682-055-73	openfda.package_ndc
ndc	package	47682-055-71	openfda.package_ndc
ndc	package	47682-045-71	openfda.package_ndc
ndc	package	47682-055-99	openfda.package_ndc
ndc	product	47682-045	openfda.product_ndc
ndc	product	47682-055	openfda.product_ndc
ndc11	package	47682005571	derived:openfda.package_ndc
ndc11	package	47682005573	derived:openfda.package_ndc
ndc11	package	47682005599	derived:openfda.package_ndc
ndc11	package	47682004571	derived:openfda.package_ndc
rxcui		1043307	openfda.rxcui
spl id		3e4cb995-be1e-a159-e063-6294a90ae6e3	id
spl set id		5744f9a2-35c6-37df-e053-2991aa0a1ca9	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 applyover large area of the body in case of deep puncture wounds, animal bites or serious burns, consult a doctor longer than 1 week unless directed by a doctor Stop use and ask 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.