Label: HOLIDAY DUST SET- alcohol kit

  • NDC Code(s): 72866-030-01, 72866-031-01, 72866-032-01, 72866-033-01
  • Packager: MERCI HANDY CORPORATION
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 23, 2024

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  • Drug Facts

  • Active ingredient

    Alcohol 67%

    Purpose

    Antiseptic

  • Use

    • for handwashing to decrease bacteria on the skin
  • Warnings

    For external use only. Flammable, keep away from fire or flame.

    Do not use

    in the eyes. In case of contact, flush eyes with water.

    Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping

  • Other information

    Store at a temperature below 110° F (43° C)

  • Inactive ingredients

    Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, D&C Red No. 30, D&C Red No. 33.

  • QUESTIONS OR COMMENTS?

    (646)-358-3432

  • Drug Facts

  • Active ingredient

    Alcohol 67% 

    Purpose

    Antiseptic

  • Use

    • for handwashing to decrease bacteria on the skin
  • Warnings

    For external use only. Flammable, keep away from fire or flame.

    Do not use

    in the eyes. In case of contact, flush eyes with water.

    Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping

  • Other information

    Store at a temperature below 110° F (43° C)

  • Inactive ingredients

    Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Benzyl Benzoate, Coumarin, Limonene, Geraniol, Chromium Oxide Greens, FD&C Yellow No. 5, FD&C Blue No. 1.

  • QUESTIONS OR COMMENTS?

    (646)-358-3432

  • Drug Facts

  • Active ingredient

    Alcohol 67%

    Purpose

    Antiseptic

  • Use

    • for handwashing to decrease bacteria on the skin
  • Warnings

    For external use only. Flammable, keep away from fire or flame.

    Do not use

    in the eyes. In case of contact, flush eyes with water.

    Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping

  • Other information

    Store at a temperature below 110° F (43° C)

  • Inactive ingredients

    Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Ferric Ferrocyanide, D&C Red No. 30, FD&C Blue No. 1, D&C Red No. 33.

  • QUESTIONS OR COMMENTS?

    (646)-358-3432

  • Package Labeling:72866-030-01

    Kit02

  • Package Labeling:72866-031-01

    Bottle

  • Package Labeling:72866-032-01

    Bottle2

  • Package Labeling:72866-033-01

    Bottle3

  • INGREDIENTS AND APPEARANCE
    HOLIDAY DUST SET 
    alcohol kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72866-030
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72866-030-011 in 1 KIT09/20/202112/31/2026
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE 30 mL
    Part 21 BOTTLE 30 mL
    Part 31 BOTTLE 30 mL
    Part 1 of 3
    HAND SANITIZER DISCO DUST 
    alcohol gel
    Product Information
    Item Code (Source)NDC:72866-031
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL67 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    MANNITOL (UNII: 3OWL53L36A)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SUCROSE (UNII: C151H8M554)  
    CORN (UNII: 0N8672707O)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72866-031-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/20/2021
    Part 2 of 3
    HAND SANITIZER FROZEN DUST 
    alcohol gel
    Product Information
    Item Code (Source)NDC:72866-032
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL67 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    COUMARIN (UNII: A4VZ22K1WT)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    GERANIOL (UNII: L837108USY)  
    CHROMIC OXIDE (UNII: X5Z09SU859)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    MANNITOL (UNII: 3OWL53L36A)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SUCROSE (UNII: C151H8M554)  
    CORN (UNII: 0N8672707O)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72866-032-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/20/2021
    Part 3 of 3
    HAND SANITIZER STAR DUST 
    alcohol gel
    Product Information
    Item Code (Source)NDC:72866-033
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL67 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    MANNITOL (UNII: 3OWL53L36A)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SUCROSE (UNII: C151H8M554)  
    CORN (UNII: 0N8672707O)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    FERRIC FERROCYANIDE (UNII: TLE294X33A)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72866-033-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/20/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/20/202112/31/2026
    Labeler - MERCI HANDY CORPORATION (118006306)
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