Label: SANITIZERSPRAY- hand sanitizer spray liquid

  • NDC Code(s): 72496-2469-1, 72496-2469-2
  • Packager: Naturich Cosmetique Labs
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 8, 2024

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

  • Active Ingredient (s)

    Ethyl Alcohol 65% Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Warnings

    For external use only. Flammable. Keep away from heat or flame.

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Other information

    • Store below 110ºF (43ºC)
  • Inactive Ingredients

    Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Camellia Sinensis Leaf Extract, Caprylic/Capric Triglyceride, Carbomer, Carthamus Tinctorius (Safflower) Seed Oil, Fragrance, Geranium Maculatum Extract, Glycerin, Lavandula Angustifolia (Lavender) Flower Extract, Propanediol, Tocopheryl Acetate, Water (Aqua).

  • Uses

    - Hand Sanitizing

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Package Label - Principal Display Panel

    Front PanelBack Panel Label

  • INGREDIENTS AND APPEARANCE
    SANITIZERSPRAY 
    hand sanitizer spray liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72496-2469
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 30 mL  in 100 mL
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72496-2469-1236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/11/2020
    2NDC:72496-2469-260 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/11/2020
    Labeler - Naturich Cosmetique Labs (124281663)
    Registrant - Naturich Cosmetique Labs (124281663)
    Establishment
    NameAddressID/FEIBusiness Operations
    Naturich Cosmetique Labs124281663manufacture(72496-2469)