Label: EGF PREMIUM WHITENING SKIN- allantoin lotion 

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  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 02/13

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  • ACTIVE INGREDIENT

    Active ingredients: Allantoin 0.5%

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  • INACTIVE INGREDIENT

    Inactive ingredients:
    Water, Sodium PCA, Betaine, Butylene Glycol, Hyaluronic acid, Portulaca Oleracea Extract, Arbutin, PEG-60 Hydrogenated Caster Oil, Beta Glucan, Alcohol, Methyl Paraben, Dipotassium Glycyrrhizate, Centella Asiatica Extract, Chamomilla Recutita Flower Extract, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra Root Extract, Polygonum Cuspidatum Root Extract, Rosemary Leaf Extract, Scutellaria Baicaliensis Root Extract, Magnolia Kobus Bark Extract, Citrus Grandis (Grapefruit) Fruit Extract, Thujopsis Dolabrata Branch Extract, Schizandra Chinensis Fruit Extract, Cirsium (Thistle) Flower/Leaf/Stem Extract, Morus Alba Bark Extract, Solanum Tuberosum (Potato) Pulp Extract, Perilla Ocymoides Seed Extract, Inonotus Obliquus (Mushroom) Extract, Propyl Paraben, Parfum, Disodium EDTA, Human Oligopeptide-1

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  • PURPOSE

    Purpose: Skin Protectant

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  • WARNINGS

    Cautions:
    1. Stop using a product if you have any unusual symptoms mentioned below. Contacting with a dermatologist is recommended rather than using it continuously and making the symptom worse.
    1) Red spots, swellings, itching, irritation.
    2) Same symptoms as above occurred after the skin spot where you applied a product was exposed to direct sunlight.
    2. Do not use for injured, eczema, or dermatitis spots.
    3. Directions for storage and handling.
    1) Remember to cover up a lid after using a product.
    2) Keep a product in unreachable place from children.
    3) Do not keep a product in too high or low temperature and under direct sunlight.

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  • KEEP OUT OF REACH OF CHILDREN

    Keep a product in unreachable place from children.

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  • INDICATIONS AND USAGE

    How to use:
    After cleansing, pour lotion enough to wet the cotton and apply from cheeks to allover face smoothly.
    Use appropriately depending on the conditions.

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  • DOSAGE AND ADMINISTRATION

    How to use:
    After cleansing, pour lotion enough to wet the cotton and apply from cheeks to allover face smoothly.
    Use appropriately depending on the conditions.

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  • PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
  • INGREDIENTS AND APPEARANCE
    EGF PREMIUM WHITENING SKIN 
    allantoin lotion
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:55133-050
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Allantoin (ALLANTOIN) Allantoin 0.75 mg  in 150 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water  
    Betaine  
    Butylene Glycol  
    Hyaluronic acid  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55133-050-01 150 mL in 1 CARTON
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 10/01/2012
    Labeler - HANBANGMEIN COSMETICS (688181385)
    Registrant - HANBANGMEIN COSMETICS (688181385)
    Establishment
    Name Address ID/FEI Business Operations
    HANBANGMEIN COSMETICS 688181385 manufacture(55133-050)
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