Label: LANBELLE LANBIO- glycerin oil

  • 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 April 1, 2018

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

  • ACTIVE INGREDIENT

    Glycerin

  • INACTIVE INGREDIENT

    Water, Adenosine, etc.

  • PURPOSE

    Skin protectant

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Apply proper amount to the skin.

  • WARNINGS

    1. Do not use in the following cases(Eczema and scalp wounds)
    2.Side Effects
    1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
    3.General Precautions
    1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
    2)This product is for exeternal use only. Do not use for internal use
    4.Storage and handling precautions
    1)If possible, avoid direct sunlight and store in cool and area of low humidity
    2)In order to maintain the quality of the product and avoid misuse
    3)Avoid placing the product near fire and store out in reach of children

  • DOSAGE & ADMINISTRATION

    for external use only


  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    LANBELLE LANBIO 
    glycerin oil
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72084-0011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    TAMANU OIL (UNII: JT3LVK84A1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72084-0011-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product03/27/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34703/27/2018
    Labeler - TAMLATAMANU Inc. (694763633)
    Registrant - TAMLATAMANU Inc. (694763633)
    Establishment
    NameAddressID/FEIBusiness Operations
    Choice Cosmetic Co., Ltd.688197261manufacture(72084-0011)
    Establishment
    NameAddressID/FEIBusiness Operations
    TAMLATAMANU Inc.694763633relabel(72084-0011)