Label: AMAZING AMPOULE- glycerin, allantoin 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 March 24, 2019

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    GLYCERIN

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  • INACTIVE INGREDIENT

    Water
    Butylene Glycol
    Glycerin
    Dipropylene Glycol
    Pentylene Glycol
    Saccharomyces/Artemisia Princeps Leaf Ferment Filtrate
    Niacinamide
    Sodium Chondroitin Sulfate
    Hexacarboxymethyl Dipeptide-12
    rh-Oligopeptide-1(10ppm)
    Butylene Glycol
    Water
    Yeast Extract
    Butylene Glycol
    Water
    Yeast Beta-Glucan
    Butylene Glycol
    Water
    Morus Alba Leaf Extract
    Water
    Human Adipocyte Conditioned Media Extract
    Phytosphingosine
    Ceramide NP
    Phospholipids
    Caprylyl Glycol
    Tropolone
    Phytosterols
    Squalane
    1,2-Hexanediol
    sh-Decapeptide-7
    sh-Octapeptide-4
    sh-Oligopeptide-9
    sh-Pentapeptide-19
    Digalloyl Tetrapeptide-19
    Tripeptide-48
    Nicotinoyl Tripeptide-1
    Palmitoyl Pentapeptide-4
    Ovalicin
    Propanediol
    Water
    Hydrolyzed Pea Protein
    Phytosterols
    Lecithin
    Olea Europaea (Olive) Fruit Oil
    Squalane
    Butyrospermum Parkii (Shea) Butter
    Ceramide NP
    Butylene Glycol
    Water
    Centella Asiatica Extract
    Polygonum Cuspidatum Root Extract
    Scutellaria Baicalensis Root Extract
    Camellia Sinensis Leaf Extract
    Glycyrrhiza Glabra (Licorice) Root Extract
    Chamomilla Recutita (Matricaria) Flower Extract
    Rosmarinus Officinalis (Rosemary) Leaf Extract
    Butylene Glycol
    Water
    Triticum Vulgare (Wheat) Seed Extract
    Butylene Glycol
    Water
    Echinacea Angustifolia Extract
    Glycerin
    Water
    Swiftlet Nest Extract
    Butylene Glycol
    Water
    Pueraria Lobata Root Extract
    Dimethicone
    Water
    Glycerin
    Butylene Glycol
    PEG-20 Glyceryl Isostearate
    Pentylene Glycol
    Tocopheryl Acetate
    Dimethicone/Vinyl Dimethicone Crosspolymer
    Diglycerin
    1,2-Hexanediol
    Butylene Glycol
    Copper Tripeptide-1
    Polysorbate 80
    Propanediol
    Aloe Barbadensis Leaf Extract
    Bioflavonoids
    Brassica Oleracea Italica (Broccoli) Extract
    Sodium Polystyrene Sulfonate
    Dipotassium Glycyrrhizate
    Cetyl Ethylhexanoate
    Dimethyl Sulfone
    Allantoin
    Adenosine
    Fragrance
    Nonapeptide-29 Hexapeptide-8
    Nonapeptide-29 Pentapeptide-4
    Panthenol
    Isopentyldiol
    Polyglyceryl-4 Oleate
    Sucrose Palmitate
    Ceramide NP
    Propanediol
    Butylene Glycol

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  • PURPOSE

    ■ to reduce effectively the intensity of skin defects

    ■ skin looks lighter

    ■ reawakened for 7 days

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  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

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  • INDICATIONS & USAGE

    spread evenly over the skin

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  • WARNINGS

    ■ if following abnormal symptoms occurs after use , stop use and consult with a skin specialist

    red specks, swelling, itching

    ■ don’t use on the part where there is injury, eczema, or dermatitis

    Keep out of reach of children

    ■ if swallowed, get medical help or contact a person control center immediately

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  • DOSAGE & ADMINISTRATION

    for external use only

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  • INGREDIENTS AND APPEARANCE
    AMAZING AMPOULE 
    glycerin, allantoin liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:72943-0002
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 3 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:72943-0002-1 40 mL in 1 BOX; Type 0: Not a Combination Product 03/24/2019
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part347 03/24/2019
    Labeler - DAONMEDICOS CO. (694819928)
    Registrant - DAONMEDICOS CO. (694819928)
    Establishment
    Name Address ID/FEI Business Operations
    DAONMEDICOS CO. 694819928 manufacture(72943-0002) , label(72943-0002) , pack(72943-0002)
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