Scented 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: Scented Hand Sanitizer
Generic name: SCENTED HAND SANITIZER
Manufacturer: Beacon Promotions, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1f95444c-7587-a07e-e063-6394a90af534
SPL ID: 48390f5d-ba29-7c28-e063-6294a90a2d7e
Version: 2
Effective date: 2026-01-12
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:38:38

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Scented Hand Sanitizer	openfda.brand_name
generic name		SCENTED HAND SANITIZER	openfda.generic_name
manufacturer name		Beacon Promotions, Inc.	openfda.manufacturer_name
ndc	package	70445-608-04	openfda.package_ndc
ndc	package	70445-608-03	openfda.package_ndc
ndc	package	70445-608-08	openfda.package_ndc
ndc	package	70445-608-05	openfda.package_ndc
ndc	package	70445-608-01	openfda.package_ndc
ndc	package	70445-608-07	openfda.package_ndc
ndc	package	70445-608-02	openfda.package_ndc
ndc	package	70445-608-09	openfda.package_ndc
ndc	package	70445-608-06	openfda.package_ndc
ndc	product	70445-608	openfda.product_ndc
ndc11	package	70445060807	derived:openfda.package_ndc
ndc11	package	70445060805	derived:openfda.package_ndc
ndc11	package	70445060803	derived:openfda.package_ndc
ndc11	package	70445060802	derived:openfda.package_ndc
ndc11	package	70445060804	derived:openfda.package_ndc
ndc11	package	70445060808	derived:openfda.package_ndc
ndc11	package	70445060809	derived:openfda.package_ndc
ndc11	package	70445060801	derived:openfda.package_ndc
ndc11	package	70445060806	derived:openfda.package_ndc
rxcui		2003712	openfda.rxcui
spl id		48390f5d-ba29-7c28-e063-6294a90a2d7e	id
spl set id		1f95444c-7587-a07e-e063-6394a90af534	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. ■ When using this product do notuse in or near the eyes. In case of contact, rinse eyes thoroughly with water. ■ Stop use andask a doctor if irritation or rash appears and lasts. ■ Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Keep out of reach of children Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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