Label: CAESARS REWARDS SANITIZER- alcohol spray

  • 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 May 25, 2020

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  • ACTIVE INGREDIENT

    Active ingredient                                  Purpose

    Alcohol                70% (w/w)      ...        Antiseptic

  • PURPOSE

    antiseptic

  • KEEP OUT OF REACH OF CHILDREN

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

  • INDICATIONS & USAGE

    avoid eye, face and broken skin.

  • WARNINGS

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

    When using this products, avoid eye, face and broken skin, if eye contact occurs, flush thoroughly with water and seek medical advise.

    Ingestion may cause alcohol poisoning. If ingested, contact your physician or pediatrician or your local poison control center.

    Stop using and ask a doctor, if irritation or redness develops.

  • DOSAGE & ADMINISTRATION

    • Squeeze onto hands and rub hands together briskly until dry.
  • INACTIVE INGREDIENT

    Water (aqua), propylene glycol, Glycerin, Aloe Barbadensis Leaf Extract, Fragrance (parfum).

  • PRINCIPAL DISPLAY PANEL

    image of label

  • INGREDIENTS AND APPEARANCE
    CAESARS REWARDS SANITIZER 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75531-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) alcohol70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75531-008-0110 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/18/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/18/2020
    Labeler - Zhejiang Ounuo Cosmetics Co., Ltd. (551868984)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Ounuo Cosmetics Co., Ltd.551868984manufacture(75531-008)
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