QUALITY CHOICE 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: QUALITY CHOICE INSTANT HAND SANITIZER
Generic name: ETHYL ALCOHOL
Manufacturer: L.e.d. Cosmetics, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 4065c34c-d1ca-49bd-9fba-dfa21011592f
SPL ID: bc10d604-7563-49ec-8cdf-f5b40264308a
Version: 3
Effective date: 2024-12-10
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 07:59:59

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		QUALITY CHOICE INSTANT HAND SANITIZER	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		L.e.d. Cosmetics, Inc.	openfda.manufacturer_name
ndc	package	77725-003-33	openfda.package_ndc
ndc	package	77725-003-02	openfda.package_ndc
ndc	package	77725-003-08	openfda.package_ndc
ndc	package	77725-003-17	openfda.package_ndc
ndc	product	77725-003	openfda.product_ndc
ndc11	package	77725000302	derived:openfda.package_ndc
ndc11	package	77725000333	derived:openfda.package_ndc
ndc11	package	77725000317	derived:openfda.package_ndc
ndc11	package	77725000308	derived:openfda.package_ndc
rxcui		581662	openfda.rxcui
spl id		bc10d604-7563-49ec-8cdf-f5b40264308a	id
spl set id		4065c34c-d1ca-49bd-9fba-dfa21011592f	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

Warning • For external use only-hands. • Flammable, keep away from heat and flame. • Discontinue if skin becomes irritated and contact a healthcare professional. When using this product • Keep out of eyes. In case of contact with eyes, flush thoroughly with water. • Do not inhale or ingest. • Avoid contact with broken skin. • Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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