SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE- benzalkonium chloride liquid 
Project Cu, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin & Aloe

symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin & Aloe


Active ingredient

Benzalkonium Chloride 0.12%

Purpose

Antibacterial

Uses

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

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

image descriptionimage description

SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64305-007
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64305-007-0712 in 1 CARTON05/23/2014
1550 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:64305-007-0824 in 1 CARTON05/23/2014
250 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/23/2014
Labeler - Project Cu, Inc. (060555505)
Establishment
NameAddressID/FEIBusiness Operations
Buckeye International, Inc.077132280manufacture(64305-007)

Revised: 1/2020
Document Id: 9c47bb32-84d9-4f7c-e053-2995a90ac881
Set id: d7be9725-4880-4a62-8f66-1d066914ad48
Version: 3
Effective Time: 20200116
 
Project Cu, Inc.