Advanced Alcohol Gel 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: Advanced Alcohol Gel Sanitizer
Generic name: ALCOHOL
Manufacturer: Betco Corporation, Ltd
Product type: HUMAN OTC DRUG
SPL set ID: a23b997c-b010-5985-e053-2995a90aadf3
SPL ID: 5b0f6af6-0cc9-aa35-e063-6294a90a584d
Version: 14
Effective date: 2026-09-09
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 06:18:40

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		505G(a)(3)	openfda.application_number
brand name		Advanced Alcohol Gel Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Betco Corporation, Ltd	openfda.manufacturer_name
ndc	package	65601-801-55	openfda.package_ndc
ndc	package	65601-801-88	openfda.package_ndc
ndc	package	65601-801-99	openfda.package_ndc
ndc	package	65601-801-29	openfda.package_ndc
ndc	package	65601-801-04	openfda.package_ndc
ndc	product	65601-801	openfda.product_ndc
ndc11	package	65601080188	derived:openfda.package_ndc
ndc11	package	65601080155	derived:openfda.package_ndc
ndc11	package	65601080104	derived:openfda.package_ndc
ndc11	package	65601080129	derived:openfda.package_ndc
ndc11	package	65601080199	derived:openfda.package_ndc
rxcui		581662	openfda.rxcui
spl id		5b0f6af6-0cc9-aa35-e063-6294a90a584d	id
spl set id		a23b997c-b010-5985-e053-2995a90aadf3	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 Warnings • For external use only. • Avoid contact with eyes. If contact occurs, rinse thoroughly with water. • FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition. • Discontinue use if irritation or redness develops. • If irritation persists for more than 72 hours, consult a physician. • 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.