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: Instant Hand Sanitizer
Generic name: ALCOHOL
Manufacturer: Water-Jel Technologies
Product type: HUMAN OTC DRUG
SPL set ID: 54e62104-8076-41db-afe5-6dc5c3563acc
SPL ID: 2b0aa634-ed75-bc52-e063-6294a90a2b50
Version: 17
Effective date: 2025-01-06
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:54

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 · 39 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Instant Hand Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Water-Jel Technologies	openfda.manufacturer_name
ndc	package	59898-420-11	openfda.package_ndc
ndc	package	59898-420-28	openfda.package_ndc
ndc	package	59898-420-04	openfda.package_ndc
ndc	package	59898-420-01	openfda.package_ndc
ndc	package	59898-420-15	openfda.package_ndc
ndc	package	59898-420-13	openfda.package_ndc
ndc	package	59898-420-02	openfda.package_ndc
ndc	package	59898-420-14	openfda.package_ndc
ndc	package	59898-420-16	openfda.package_ndc
ndc	package	59898-420-10	openfda.package_ndc
ndc	package	59898-420-12	openfda.package_ndc
ndc	package	59898-420-03	openfda.package_ndc
ndc	package	59898-420-36	openfda.package_ndc
ndc	package	59898-420-33	openfda.package_ndc
ndc	package	59898-420-17	openfda.package_ndc
ndc	product	59898-420	openfda.product_ndc
ndc11	package	59898042014	derived:openfda.package_ndc
ndc11	package	59898042036	derived:openfda.package_ndc
ndc11	package	59898042001	derived:openfda.package_ndc
ndc11	package	59898042003	derived:openfda.package_ndc
ndc11	package	59898042033	derived:openfda.package_ndc
ndc11	package	59898042012	derived:openfda.package_ndc
ndc11	package	59898042011	derived:openfda.package_ndc
ndc11	package	59898042002	derived:openfda.package_ndc
ndc11	package	59898042013	derived:openfda.package_ndc
ndc11	package	59898042010	derived:openfda.package_ndc
ndc11	package	59898042015	derived:openfda.package_ndc
ndc11	package	59898042017	derived:openfda.package_ndc
ndc11	package	59898042004	derived:openfda.package_ndc
ndc11	package	59898042016	derived:openfda.package_ndc
ndc11	package	59898042028	derived:openfda.package_ndc
rxcui		581660	openfda.rxcui
spl id		2b0aa634-ed75-bc52-e063-6294a90a2b50	id
spl set id		54e62104-8076-41db-afe5-6dc5c3563acc	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 For external use only Flammable, keep away from fire or flame When using this product do not use in the eyes discontinue use if irritation and redness develops. If condition persists for more than 72 hours consult a doctor. 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.