SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE- benzalkonium chloride liquid

symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe by

Drug Labeling and Warnings

symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe by is a Otc medication manufactured, distributed, or labeled by Project Cu, Inc., Buckeye International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin & Aloe

Active ingredient

Benzalkonium Chloride 0.12%

Purpose

Antibacterial

Uses

• Hand sanitizer to help reduce bacteria on the skin could cause disease
  
• Recommended for repeated use
  

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 physician.

Keep out of reach of children.

If swallowed, call a physician or Poison Control Center immediately.

Directions

• Dispense an adequate amount of hand sanitizer

• Rub hands together until completely dry
  

Inactive ingredients

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

Questions?

Call: Buckeye International, Inc. - 314-291-1900 Monday through Friday - 8:00 a.m. to 5:00 p.m. CST

Representative Labeling

INGREDIENTS AND APPEARANCE

SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64305-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.2 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
EDETATE SODIUM (UNII: MP1J8420LU)
ALLANTOIN (UNII: 344S277G0Z)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64305-007-07	12 in 1 CARTON	05/23/2014
1		550 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 64305-007-08	24 in 1 CARTON	05/23/2014
2		50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/23/2014

Labeler - Project Cu, Inc. (060555505)

Establishment
Name	Address	ID/FEI	Business Operations
Buckeye International, Inc.		077132280	manufacture(64305-007)