Symmetry Foaming Hand Sanitizer-Fragrance Free with Aloe and Vitamin E

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-Fragrance Free with Aloe and Vitamin E
Generic name: ALCOHOL
Manufacturer: Buckeye International, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 00a2c2b4-b540-4acc-86b9-b4dfb4e8695b
SPL ID: 3131222a-d13e-4953-e063-6294a90a9489
Version: 7
Effective date: 2025-03-25
Source export date: 2026-10-30
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/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:34:17

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 · 25 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-Fragrance Free with Aloe and Vitamin E	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Buckeye International, Inc.	openfda.manufacturer_name
ndc	package	30805-009-10	openfda.package_ndc
ndc	package	30805-009-11	openfda.package_ndc
ndc	package	30805-009-08	openfda.package_ndc
ndc	package	30805-009-07	openfda.package_ndc
ndc	package	30805-009-05	openfda.package_ndc
ndc	package	30805-009-04	openfda.package_ndc
ndc	package	30805-009-09	openfda.package_ndc
ndc	package	30805-009-13	openfda.package_ndc
ndc	product	30805-009	openfda.product_ndc
ndc11	package	30805000913	derived:openfda.package_ndc
ndc11	package	30805000905	derived:openfda.package_ndc
ndc11	package	30805000910	derived:openfda.package_ndc
ndc11	package	30805000908	derived:openfda.package_ndc
ndc11	package	30805000904	derived:openfda.package_ndc
ndc11	package	30805000909	derived:openfda.package_ndc
ndc11	package	30805000911	derived:openfda.package_ndc
ndc11	package	30805000907	derived:openfda.package_ndc
rxcui		616763	openfda.rxcui
spl id		3131222a-d13e-4953-e063-6294a90a9489	id
spl set id		00a2c2b4-b540-4acc-86b9-b4dfb4e8695b	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#

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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.