FDA.reportPublic FDA data

Symmetry Non-Alcohol Foaming Hand Sanitizer

Manufacturer
Buckeye International, Inc.
Effective date
2010-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:51:51

Label at a glance#

ProductSymmetry Non-Alcohol Foaming Hand Sanitizer
Active ingredientBenzalkonium Chloride
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium Chloride 0.24%

INDICATIONS & USAGE SECTION

Uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease

Recommended for repeated use

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product do not use in or near eyes.

If in eyes, flush thoroughly with water.

ADVERSE REACTIONS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

Dispense an adequate amount of hand sanitizer

Rub hands together until completely dry

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water (Aqua), Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Allantoin, Fragrance (Parfum), Aloe Barbadensis Leaf Juice, Methylchloroisothiazolinone, Methylisothiazolinone

OTC - QUESTIONS SECTION

Questions?

Call: Buckeye International, Inc. 314-291-1900

Monday through Friday 8:00 to 5:00 p.m. CST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

For General Hand Sanitizing

Symmetry Non-Alcohol Foaming Hand Sanitizer

with Allantoin and Aloe

Product 90150050

Net Contents 550 ml (18.6 fl oz)

container labelcontainer label

OTC - PURPOSE SECTION

Purpose

Antibacterial

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
30805-007-022025-12-02C16284748780-19d75b9d1-0add-f424-e053-dadaa90a57ceDrug Facts
30805-007-072025-12-02C16284748780-19d75b9d1-0add-f424-e053-dadaa90a57ceDrug Facts
30805-007-022020-01-31C16284748780-19d75b9d1-0add-f424-e053-dadaa90a57ceDrug Facts
30805-007-072020-01-31C16284748780-19d75b9d1-0add-f424-e053-dadaa90a57ceDrug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30805-007SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [BUCKEYE INTERNATIONAL, INC.]2Legacy NDC20110128_f86a95a4-2f38-4ef4-882e-d2feb3aefd96.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W72
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y2
AllantoinINACTIVE INGREDIENT344S277G0Z2
Aloe Vera LeafINACTIVE INGREDIENTZY81Z83H0X2
Cocamidopropyl BetaineINACTIVE INGREDIENT5OCF3O11KX2
EDETATE SODIUMINACTIVE INGREDIENTMP1J8420LU2
LAURAMINE OXIDEINACTIVE INGREDIENT4F6FC4MI8W2
METHYLCHLOROISOTHIAZOLINONEINACTIVE INGREDIENTDEL7T5QRPN2
MethylisothiazolinoneINACTIVE INGREDIENT229D0E1QFA2
WaterINACTIVE INGREDIENT059QF0KO0R2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30805-00730805-007-02, 30805-007-07

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
Cocamidopropyl Betaine5OCF3O11KXIACT
Allantoin344S277G0ZIACT
Aloe Vera LeafZY81Z83H0XIACT
Methylisothiazolinone229D0E1QFAIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
EDETATE SODIUMMP1J8420LUIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 15 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LAURAMINE OXIDELAURAMINE OXIDE4F6FC4MI8WSPONGE / TOPICALNAExact identifier — unii candidate
2 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUSOAP / TOPICAL0.12 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUINJECTION / INTRAMUSCULAR0.01 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUEMULSION / OPHTHALMIC0.02 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
LAURAMINE OXIDELAURAMINE OXIDE4F6FC4MI8WSOLUTION / TOPICAL3.5 %w/vExact identifier — unii candidate
2 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUSPONGE / TOPICAL0.14 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUSHAMPOO / TOPICAL1.33 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUTABLET / ORAL5 mgExact identifier — unii candidate
12 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUSOLUTION / OPHTHALMIC0.1 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
AllantoinALLANTOIN344S277G0ZGEL / TOPICAL8 mgExact identifier — unii candidate
EDETATE SODIUMEDETATE SODIUMMP1J8420LULOTION / TOPICAL0.17 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUINJECTION, SOLUTION / INTRAVENOUS0.04 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUINJECTION / INTRAVENOUS0.01 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUSOLUTION / TOPICAL0.3 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
EDETATE SODIUMEDETATE SODIUMMP1J8420LUCAPSULE / ORAL1 mgExact identifier — unii candidate
12 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
41d8794a-a3a8-32c1-e063-6394a90a39a1f86a95a4-2f38-4ef4-882e-d2feb3aefd962025-10-23Warnings, Adverse reactionsExact identifier
spl set id: f86a95a4-2f38-4ef4-882e-d2feb3aefd96

Reported adverse events (FAERS/openFDA)#

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