SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER- benzalkonium chloride liquid

Symmetry Non-Alcohol Foaming Hand Sanitizer by

Drug Labeling and Warnings

Symmetry Non-Alcohol Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Buckeye International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Benzalkonium Chloride 0.24%

INDICATIONS & USAGE

Uses

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

Recommended for repeated use

WARNINGS

Warnings

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.

DOSAGE & ADMINISTRATION

Directions

Dispense an adequate amount of hand sanitizer

Rub hands together until completely dry

INACTIVE INGREDIENT

Inactive ingredients

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

QUESTIONS

Questions?

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

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

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)

PURPOSE

Purpose

Antibacterial

INGREDIENTS AND APPEARANCE

SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 30805-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	0.24 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Allantoin (UNII: 344S277G0Z)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Methylisothiazolinone (UNII: 229D0E1QFA)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30805-007-02	1250 mL in 1 BAG
2	NDC: 30805-007-07	550 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/09/2009

Labeler - Buckeye International, Inc. (077132280)

Establishment
Name	Address	ID/FEI	Business Operations
Buckeye International, Inc.		077132280	manufacture