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

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

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  • Uses

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

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  • Directions

    • Dispense an adequate amount of hand sanitizer
    • Rub hands together until completely dry
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  • Inactive ingredients


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

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  • Questions?

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

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  • 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, Inc. (060555505)
    Establishment
    Name Address ID/FEI Business Operations
    Buckeye International, Inc. 077132280 manufacture(64305-007)
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