Label: CLOUD9 HAND SANITIZER S- ethyl alcohol liquid

  • 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 April 25, 2020

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  • Active Ingredient(s)

    Ethyl alcohol 80%

  • Purpose

    Antiseptic

  • Uses

    Hand sanitizer to help reduce bacteria on hands.
    Recommended for repeated use.

  • Warnings

    For external use only.

    Flammable - Keep away from fire or flame

  • When using this product

    • Keep out of eyes, ear and mouth.
    • In case of contact with eyes, rinse eyes thoroughly with water.
  • Stop use and ask a doctor

    if irritation and redness develop or increase.

  • Keep out of reach of children

    if swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply a small amount onto hands and rub briskly until dry.
    • Supervise children in the use of this product.
  • Other information

    • Store at 15-30ºC (59-86ºF)
    • Avoid freezing and excessive heat above 40 ºC (104ºF)
  • Inactive ingredients

    Water, Glycerin, Hydrogen Peroxide

  • Package Label - Principal Display Panel

    500 mL NDC: 73330-0012-1

    500ml label

    100 mL NDC: 73330-0012-2

    100ml label

  • INGREDIENTS AND APPEARANCE
    CLOUD9 HAND SANITIZER S 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73330-0013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.8 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73330-0013-1500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/30/2020
    2NDC:73330-0013-2100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/30/2020
    Labeler - COSNINE Inc (694607163)
    Establishment
    NameAddressID/FEIBusiness Operations
    COSNINE, INC.694607163manufacture(73330-0013)
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