Symmetry Foaming 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 Foaming Hand Sanitizer
Generic name: ALCOHOL
Manufacturer: Buckeye International, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: bcab4842-50ff-4c7f-8b85-0126f4b585b0
SPL ID: 1defd1cf-e659-0400-e063-6294a90a39de
Version: 5
Effective date: 2024-07-23
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:13

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 Foaming Hand Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Buckeye International, Inc.	openfda.manufacturer_name
ndc	package	30805-003-04	openfda.package_ndc
ndc	package	30805-003-05	openfda.package_ndc
ndc	package	30805-003-09	openfda.package_ndc
ndc	package	30805-003-07	openfda.package_ndc
ndc	package	30805-003-08	openfda.package_ndc
ndc	package	30805-003-10	openfda.package_ndc
ndc	package	30805-003-03	openfda.package_ndc
ndc	product	30805-003	openfda.product_ndc
ndc11	package	30805000307	derived:openfda.package_ndc
ndc11	package	30805000303	derived:openfda.package_ndc
ndc11	package	30805000305	derived:openfda.package_ndc
ndc11	package	30805000308	derived:openfda.package_ndc
ndc11	package	30805000310	derived:openfda.package_ndc
ndc11	package	30805000304	derived:openfda.package_ndc
ndc11	package	30805000309	derived:openfda.package_ndc
rxcui		616763	openfda.rxcui
spl id		1defd1cf-e659-0400-e063-6294a90a39de	id
spl set id		bcab4842-50ff-4c7f-8b85-0126f4b585b0	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.