Label: SANSPRAY-NA- non-alcohol antibacterial hand sanitizer spray

  • NDC Code(s): 70445-606-01
  • Packager: Beacon Promotions, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 3, 2024

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  • Purpose

    Antiseptic

  • Warnings:

    For external use only. Flammable. Keep away from heat or flame. Keep out of eyes, ears
    & mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask doctor if
    redness or irritation develop and persist for more than 72 hours. Keep out of reach of children.
    If swallowed, get medical help or contact a Poison Control Center right away.
    Do not use on children less than 2 months of age. Do not use on open skin wounds.

  • Directions

    Spray enough product on hands to cover
    all surfaces. Rub hands together until dry.

  • Inactive Ingredient:

    Water, Aloe Vera, Glycerin, Propylene Glycol, Tocopherol, Lemon Fragrance.

  • Purpose

    Anticeptic

  • Drug Facts

    Active Ingredient Purpose
    Benzalkonium Chloride (0.1%)

    Spray enough product on hands to cover
    all surfaces. Rub hands together until dry.

  • Keep out of reach of children

    keep out of reach of children

  • PRINCIPAL DISPLAY PANEL

    SSNA

  • INGREDIENTS AND APPEARANCE
    SANSPRAY-NA 
    non-alcohol antibacterial hand sanitizer spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70445-606
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE (UNII: V5VD430YW9)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70445-606-019.76 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/03/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/03/2024
    Labeler - Beacon Promotions, Inc. (119056382)
    Establishment
    NameAddressID/FEIBusiness Operations
    Beacon Promotions Inc.119056382manufacture(70445-606)
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