Label: MAGIC POUCH- alcohol kit

  • NDC Code(s): 72866-002-30, 72866-003-30, 72866-009-30, 72866-011-01
  • Packager: Merci Handy Corporation
  • 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 November 29, 2022

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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

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

    Water (Aqua), Fragrance (Parfum), Aloe Vera Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
    Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch, Denatonium Benzoate, Tocopheryl Acetate,
    Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Fluorphlogopite, Coumarin, Limonene, Alpha-Isomethyl Ionone, Cinnamyl Alcohol, Isoeugenol, Titanium Dioxide, FD&C Yellow No. 5, Iron Oxides FD&C Red No. 4.

  • 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

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

  • QUESTIONS OR COMMENTS?

    (646)-358-3432

  • Package Labeling:Kit

    Kit

  • Package Labeling:NAMASTE

    Box

  • Package Labeling:GLITTER FEVER

    Box2

  • Package Labeling:UNICORN EDITION

    Box3

  • INGREDIENTS AND APPEARANCE
    MAGIC POUCH 
    alcohol kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72866-011
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72866-011-011 in 1 KIT10/15/202006/30/2025
    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, NAMASTE 
    alcohol gel
    Product Information
    Item Code (Source)NDC:72866-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    MANNITOL (UNII: 3OWL53L36A)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SUCROSE (UNII: C151H8M554)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    FERRIC FERROCYANIDE (UNII: TLE294X33A)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72866-002-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/15/2020
    Part 2 of 3
    HAND SANITIZER, GLITTER FEVER 
    alcohol gel
    Product Information
    Item Code (Source)NDC:72866-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 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)  
    COUMARIN (UNII: A4VZ22K1WT)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    CINNAMYL ALCOHOL (UNII: SS8YOP444F)  
    ISOEUGENOL (UNII: 5M0MWY797U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72866-009-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/15/2020
    Part 3 of 3
    HAND SANITIZER, UNICORN EDITION 
    alcohol gel
    Product Information
    Item Code (Source)NDC:72866-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    MANNITOL (UNII: 3OWL53L36A)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SUCROSE (UNII: C151H8M554)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    COUMARIN (UNII: A4VZ22K1WT)  
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72866-003-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/15/202006/30/2025
    Labeler - Merci Handy Corporation (118006306)
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