Symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe

Manufacturer: Buckeye International, Inc.
Effective date: 2024-11-15
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:37:48

Label at a glance#

ProductSymmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Contacts and useful links#

PhoneLabel contact314-291-1900

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium Chloride 0.12%

OTC - PURPOSE SECTION

Purpose

Antibacterial

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 8:00to 5:00 p.m. CST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

For General Hand Sanitizing

Symmetry

Non-Alcohol Foaming

Hand Sanitizer

w/ Allantoin and Aloe

Product # 90153000

Net Content 1000 ml (33.8 fl oz)

container label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1046310	Benzalkonium (Topical)	benzalkonium chloride 1.2 MG/ML Topical Foam	SCD Active
1052949	Benzalkonium (Topical)	benzalkonium chloride 1.2 MG/ML Topical Solution	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046310	benzalkonium chloride 0.12 % Topical Foam	PSN	3
1046310	benzalkonium chloride 1.2 MG/ML Topical Foam	SCD	3
1046310	benzalkonium chloride 0.12 % Topical Foam	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
30805-010-02	Symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe	1250 mL in 1 BAG	SOLUTION	1250	3
30805-010-05	Symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe	50 mL in 1 BOTTLE, PUMP	SOLUTION	50	3
30805-010-07	Symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe	550 mL in 1 BOTTLE, PUMP	SOLUTION	550	3
30805-010-09	Symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe	1000 mL in 1 BAG	SOLUTION	1000	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
30805-010	SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE (BENZALKONIUM CHLORIDE) SOLUTION [BUCKEYE INTERNATIONAL, INC.]	3	Current NDC, Legacy NDC, 4 package rows	20241120_2750f62c-e650-428a-b070-5c13ff8e378e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Benzalkonium Chloride	ACTIVE INGREDIENT	F5UM2KM3W7	1
Benzalkonium	ACTIVE MOIETY	7N6JUD5X6Y	1
Allantoin	INACTIVE INGREDIENT	344S277G0Z	1
Aloe Vera Leaf	INACTIVE INGREDIENT	ZY81Z83H0X	1
Cocamidopropyl Betaine	INACTIVE INGREDIENT	5OCF3O11KX	1
EDETATE SODIUM	INACTIVE INGREDIENT	MP1J8420LU	1
LAURAMINE OXIDE	INACTIVE INGREDIENT	4F6FC4MI8W	1
METHYLCHLOROISOTHIAZOLINONE	INACTIVE INGREDIENT	DEL7T5QRPN	1
Methylisothiazolinone	INACTIVE INGREDIENT	229D0E1QFA	1
Water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

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

Symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe
Benzalkonium Chloride
WATER
COCAMIDOPROPYL BETAINE
LAURAMINE OXIDE
EDETATE SODIUM
ALLANTOIN
ALOE VERA LEAF
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
30805-010	30805-010-02, 30805-010-05, 30805-010-07, 30805-010-09

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
EDETATE SODIUM	MP1J8420LU	IACT
ALLANTOIN	344S277G0Z	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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 ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Allantoin	ALLANTOIN	344S277G0Z	GEL / TOPICAL		8 mg	Exact identifier — unii+route 5 equally ranked IID candidates
Allantoin	ALLANTOIN	344S277G0Z	GEL / TOPICAL		8 mg	Exact identifier — unii+route 5 equally ranked IID candidates
Allantoin	ALLANTOIN	344S277G0Z	GEL / TOPICAL		8 mg	Exact identifier — unii+route 5 equally ranked IID candidates
LAURAMINE OXIDE	LAURAMINE OXIDE	4F6FC4MI8W	SOLUTION / TOPICAL	3.5 %w/v		Exact identifier — unii+route+dosage form 5 equally ranked IID candidates
Allantoin	ALLANTOIN	344S277G0Z	GEL / TOPICAL		8 mg	Exact identifier — unii+route 5 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 5 equally ranked IID candidates
LAURAMINE OXIDE	LAURAMINE OXIDE	4F6FC4MI8W	SOLUTION / TOPICAL	3.5 %w/v		Exact identifier — unii+route+dosage form 5 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 5 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 5 equally ranked IID candidates
LAURAMINE OXIDE	LAURAMINE OXIDE	4F6FC4MI8W	SOLUTION / TOPICAL	3.5 %w/v		Exact identifier — unii+route+dosage form 5 equally ranked IID candidates
Allantoin	ALLANTOIN	344S277G0Z	GEL / TOPICAL		8 mg	Exact identifier — unii+route 5 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 5 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 5 equally ranked IID candidates
LAURAMINE OXIDE	LAURAMINE OXIDE	4F6FC4MI8W	SOLUTION / TOPICAL	3.5 %w/v		Exact identifier — unii+route+dosage form 5 equally ranked IID candidates
LAURAMINE OXIDE	LAURAMINE OXIDE	4F6FC4MI8W	SOLUTION / TOPICAL	3.5 %w/v		Exact identifier — unii+route+dosage form 5 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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe	BENZALKONIUM CHLORIDE	Buckeye International, Inc.	2750f62c-e650-428a-b070-5c13ff8e378e	2024-11-15	Warnings, Adverse reactions	Exact identifier ndc (package): 30805-010-07 ndc (package): 30805-010-02 ndc (package): 30805-010-09 ndc (package): 30805-010-05 ndc (product): 30805-010 ndc11 (package): 30805001007 ndc11 (package): 30805001009 ndc11 (package): 30805001005 ndc11 (package): 30805001002 spl id: 26f6d4e6-ec46-4d11-e063-6294a90abaa7 spl set id: 2750f62c-e650-428a-b070-5c13ff8e378e

Reported adverse events (FAERS/openFDA)#

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