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

  • NDC Code(s): 64305-007-07, 64305-007-08
  • Packager: Project, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated October 31, 2018

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  • 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

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  • INGREDIENTS AND APPEARANCE
    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, Inc. (060555505)
    Establishment
    NameAddressID/FEIBusiness Operations
    Buckeye International, Inc.077132280manufacture(64305-007)