Smart San 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: Smart San Hand Sanitizer
Generic name: ALCOHOL
Manufacturer: Best Sanitizers, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b76459d8-747b-86f9-e053-2a95a90ab654
SPL ID: 288c7845-601d-0f59-e063-6394a90a61dc
Version: 2
Effective date: 2024-12-12
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:36:32

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		Smart San Hand Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Best Sanitizers, Inc.	openfda.manufacturer_name
ndc	package	59900-121-01	openfda.package_ndc
ndc	package	59900-121-02	openfda.package_ndc
ndc	package	59900-121-05	openfda.package_ndc
ndc	package	59900-121-04	openfda.package_ndc
ndc	package	59900-121-03	openfda.package_ndc
ndc	product	59900-121	openfda.product_ndc
ndc11	package	59900012102	derived:openfda.package_ndc
ndc11	package	59900012105	derived:openfda.package_ndc
ndc11	package	59900012101	derived:openfda.package_ndc
ndc11	package	59900012103	derived:openfda.package_ndc
ndc11	package	59900012104	derived:openfda.package_ndc
rxcui		1052526	openfda.rxcui
spl id		288c7845-601d-0f59-e063-6394a90a61dc	id
spl set id		b76459d8-747b-86f9-e053-2a95a90ab654	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 or near eyes use in a well-ventilated area Stop use and consult a doctor if irritation or redness develops. Keep out of reach of children. If swallowed, seek medical attention or contact Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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