SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE- benzalkonium chloride liquid 
Project, 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 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, Inc. (060555505)
Establishment
Name Address ID/FEI Business Operations
Buckeye International, Inc. 077132280 manufacture(64305-007)

Revised: 10/2018
Document Id: 798b9f79-d4cb-633c-e053-2a91aa0ad2cf
Set id: d7be9725-4880-4a62-8f66-1d066914ad48
Version: 2
Effective Time: 20181031
 
Project, Inc.