Label: IMPLAHEAL P.OCREAM- illite, acetyl glucosamine, dimethyl sulfon cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 4, 2020

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

  • ACTIVE INGREDIENT

    illite, acetyl glucosamine, dimethyl sulfone, hydrolyzed sponge, morinda citrifolia extract,

    Olea Europaea (Olive) Fruit Oil
    Lavandula Angustifolia (Lavender) Oil
    Pinus Sylvestris Leaf Oil
    Cananga Odorata Flower Oil
    Rosmarinus Officinalis (Rosemary) Leaf Oil
    Artemisia Vulgaris Oil
    Pelargonium Graveolens Flower Oil
    Melaleuca Alternifolia (Tea Tree)Leaf Oil

  • INACTIVE INGREDIENT

    Water
    Glycerin
    Ceramide 3
    Hydrogenated Lecithin
    Cyclopentasiloxane
    Dimethiconol

    etc

  • PURPOSE

    to penetrate into skin deeply and helps improvement

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    after getting proper amount, let absorption to the improved part by massage

  • WARNINGS

    Warning: 1. Do not use if you have any of following problems during use: ① Rash, red spots, swelling, irritation ② If the application site has any of the above problems due to direct sunlight

    2. Precautions for storage and handling ① Close the cap after use ② Keep out of reach of children ③ Do not store under high or low temperature and direct sunlight.

    If you continue to use the product, the symptoms may worsen. Stop use and ask a doctor if abnormality occurs.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    IMPLAHEAL P.OCREAM 
    illite, acetyl glucosamine, dimethyl sulfon cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72368-0007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    N-ACETYLGLUCOSAMINE (UNII: V956696549) (N-ACETYLGLUCOSAMINE - UNII:V956696549) N-ACETYLGLUCOSAMINE2 g  in 100 mL
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) (DIMETHYL SULFONE - UNII:9H4PO4Z4FT) DIMETHYL SULFONE1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72368-0007-180 mL in 1 TUBE; Type 0: Not a Combination Product12/16/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/16/2019
    Labeler - Threedayslove Co., Ltd. (693724138)
    Registrant - Threedayslove Co., Ltd. (693724138)
    Establishment
    NameAddressID/FEIBusiness Operations
    Threedayslove Co., Ltd.693724138manufacture(72368-0007) , pack(72368-0007) , label(72368-0007)