5259 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: 5259 HAND SANITIZER
Generic name: ETHYL ALCOHOL
Manufacturer: Innovation Specialties
Product type: HUMAN OTC DRUG
SPL set ID: 3923fe13-0e57-406a-afb9-3e9cef263dab
SPL ID: 1cee8d76-1f8e-14b4-e063-6294a90afc0e
Version: 3
Effective date: 2024-07-10
Source export date: 2026-10-30
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:33:44

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		5259 HAND SANITIZER	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		Innovation Specialties	openfda.manufacturer_name
ndc	package	76138-120-04	openfda.package_ndc
ndc	product	76138-120	openfda.product_ndc
ndc11	package	76138012004	derived:openfda.package_ndc
rxcui		581660	openfda.rxcui
spl id		1cee8d76-1f8e-14b4-e063-6294a90afc0e	id
spl set id		3923fe13-0e57-406a-afb9-3e9cef263dab	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. For external use only. Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours. 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.