Label: MARQUIS GEL FORMULA gel

  • NDC Code(s): 76585-010-11, 76585-010-12, 76585-010-13, 76585-010-14, view more
    76585-010-15, 76585-010-16, 76585-010-17, 76585-010-18, 76585-010-20
  • Packager: Marquis XT LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 29, 2024

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  • Active Ingredients

    Alcohol 70% v/v

    Purpose Antiseptic

  • Purpose

    Antiseptic

  • Stop use and ask a doctor if

    irritation or rash occurs. These may be signs of a serious condition.

  • Use

    Hand sanitizer to help reduce bacteria on the skin that potentially can cause disease.

    For use when soap and water are unavailable.

  • Warnings

    For external use only.

    Keep away from heat or flame.

  • Do not use

    in children less than 2 months of age

    on open skin wounds

    in eyes

  • When using this product

    keep out of eyes, ears, and mouth

    in case of contactwith eyes, rinse eyes thoroughly with water

  • Kep out of reach of children

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

  • Directions

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

    Supervise children under age 6 when using this product to avoid swallowing.

  • Other Information

    Store between 59-86 F (15-30C)

    Avoid freezing and excessive heat above 104F (40C)

  • Inactive Ingredients

    acrylate copolymer, aloe, denatonium benzoate, fragrance, propylene glycol, water

  • Package Label

    0100

    Gel 010

  • INGREDIENTS AND APPEARANCE
    MARQUIS GEL FORMULA 
    marquis gel formula gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76585-010
    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
    LINALOOL, (+)- (UNII: F4VNO44C09) 0.3 mL  in 100 mL
    DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O) 0.00035 mL  in 100 mL
    METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C) 1.1 mL  in 100 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.005 mL  in 100 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 1 mL  in 100 mL
    CUMINYL ACETALDEHYDE (UNII: WSW8QXE6HG) 0.3 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76585-010-173785 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    2NDC:76585-010-11473 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    3NDC:76585-010-13236 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    4NDC:76585-010-14946 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    5NDC:76585-010-1512113 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    6NDC:76585-010-121040875 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    7NDC:76585-010-18355 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    8NDC:76585-010-1618927 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    9NDC:76585-010-2059 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/01/2020
    Labeler - Marquis XT LLC (117496233)
    Establishment
    NameAddressID/FEIBusiness Operations
    Marquis XT LLC117496233manufacture(76585-010)
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