Decon Hand Instant Hand Sanitizer

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: Decon Hand Instant Hand Sanitizer
Generic name: ALCOHOL
Manufacturer: Veltek Associates, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b0fb3d45-a5c9-4d3c-a840-1b7564ecb3f8
SPL ID: 07ca66ec-a987-7d19-e063-6294a90ae868
Version: 11
Effective date: 2023-10-15
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:32:07

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Decon Hand Instant Hand Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Veltek Associates, Inc.	openfda.manufacturer_name
ndc	package	64307-001-06	openfda.package_ndc
ndc	package	64307-001-05	openfda.package_ndc
ndc	package	64307-001-04	openfda.package_ndc
ndc	package	64307-001-09	openfda.package_ndc
ndc	package	64307-001-02	openfda.package_ndc
ndc	package	64307-001-10	openfda.package_ndc
ndc	product	64307-001	openfda.product_ndc
ndc11	package	64307000102	derived:openfda.package_ndc
ndc11	package	64307000106	derived:openfda.package_ndc
ndc11	package	64307000109	derived:openfda.package_ndc
ndc11	package	64307000105	derived:openfda.package_ndc
ndc11	package	64307000110	derived:openfda.package_ndc
ndc11	package	64307000104	derived:openfda.package_ndc
rxcui		1100016	openfda.rxcui
spl id		07ca66ec-a987-7d19-e063-6294a90ae868	id
spl set id		b0fb3d45-a5c9-4d3c-a840-1b7564ecb3f8	set_id
unii		3K9958V90M	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 Flammable, keep away from fire or flame when using this product For External Use Only Do not use in eyes. In case of eye contact, flush with water for 15 minutes. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor. Avoid contact with broken skin. 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.