SnugZ Hand Sanitizer Gel

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: SnugZ Hand Sanitizer Gel
Generic name: HAND SANITIZER GEL
Manufacturer: SnugZ/USA, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 69bc7a80-0898-4c08-e053-2a91aa0a87a9
SPL ID: 4720ba94-cc7c-fec5-e063-6394a90a59cb
Version: 11
Effective date: 2025-12-29
Source export date: 2026-11-06
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/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:10:20

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 · 35 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		SnugZ Hand Sanitizer Gel	openfda.brand_name
generic name		HAND SANITIZER GEL	openfda.generic_name
manufacturer name		SnugZ/USA, LLC	openfda.manufacturer_name
ndc	package	76309-301-04	openfda.package_ndc
ndc	package	76309-301-91	openfda.package_ndc
ndc	package	76309-301-01	openfda.package_ndc
ndc	package	76309-301-19	openfda.package_ndc
ndc	package	76309-301-88	openfda.package_ndc
ndc	package	76309-301-02	openfda.package_ndc
ndc	package	76309-301-81	openfda.package_ndc
ndc	package	76309-301-61	openfda.package_ndc
ndc	package	76309-301-99	openfda.package_ndc
ndc	package	76309-301-62	openfda.package_ndc
ndc	package	76309-301-05	openfda.package_ndc
ndc	package	76309-301-08	openfda.package_ndc
ndc	package	76309-301-51	openfda.package_ndc
ndc	product	76309-301	openfda.product_ndc
ndc11	package	76309030199	derived:openfda.package_ndc
ndc11	package	76309030102	derived:openfda.package_ndc
ndc11	package	76309030101	derived:openfda.package_ndc
ndc11	package	76309030181	derived:openfda.package_ndc
ndc11	package	76309030119	derived:openfda.package_ndc
ndc11	package	76309030188	derived:openfda.package_ndc
ndc11	package	76309030162	derived:openfda.package_ndc
ndc11	package	76309030105	derived:openfda.package_ndc
ndc11	package	76309030161	derived:openfda.package_ndc
ndc11	package	76309030191	derived:openfda.package_ndc
ndc11	package	76309030108	derived:openfda.package_ndc
ndc11	package	76309030104	derived:openfda.package_ndc
ndc11	package	76309030151	derived:openfda.package_ndc
rxcui		581662	openfda.rxcui
spl id		4720ba94-cc7c-fec5-e063-6394a90a59cb	id
spl set id		69bc7a80-0898-4c08-e053-2a91aa0a87a9	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. Do not use on damaged or broken skin. Keep out of eyes . Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If product is 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.