Symmetry 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: Symmetry Hand Sanitizer
Generic name: ALCOHOL
Manufacturer: Buckeye International, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 7f38c146-b5d3-489e-b1c7-89dcea2c18a8
SPL ID: 424f265a-d5af-56fd-e063-6394a90a66c4
Version: 7
Effective date: 2025-10-29
Source export date: 2026-10-27
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/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:49:44

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Symmetry Hand Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Buckeye International, Inc.	openfda.manufacturer_name
ndc	package	30805-001-09	openfda.package_ndc
ndc	package	30805-001-12	openfda.package_ndc
ndc	package	30805-001-01	openfda.package_ndc
ndc	package	30805-001-07	openfda.package_ndc
ndc	package	30805-001-03	openfda.package_ndc
ndc	package	30805-001-06	openfda.package_ndc
ndc	package	30805-001-04	openfda.package_ndc
ndc	product	30805-001	openfda.product_ndc
ndc11	package	30805000101	derived:openfda.package_ndc
ndc11	package	30805000112	derived:openfda.package_ndc
ndc11	package	30805000103	derived:openfda.package_ndc
ndc11	package	30805000104	derived:openfda.package_ndc
ndc11	package	30805000106	derived:openfda.package_ndc
ndc11	package	30805000109	derived:openfda.package_ndc
ndc11	package	30805000107	derived:openfda.package_ndc
rxcui		247835	openfda.rxcui
spl id		424f265a-d5af-56fd-e063-6394a90a66c4	id
spl set id		7f38c146-b5d3-489e-b1c7-89dcea2c18a8	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 not use in or near eyes. If in eyes, flush thoroughly with water. If irritation or rash appears and persists, stop use and see a physician. Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

If irritation or rash appears and persists, stop use and see a physician.

Reported adverse events (FAERS/openFDA)#

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