Label: LETOMINT- clove tablet

  • 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 June 18, 2011

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

  • ACTIVE INGREDIENT

    active ingredient: clove
  • INACTIVE INGREDIENT

    inactive ingredient:  aluminium sulfate, garlic, polyethylens glycols, vitamin E, aloe, water, sepia esculenta, galla rhois
  • PURPOSE

    improvement of vaginal discharge, leukorrhea, vperiod pain and menstrual irregularity
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children
  • INDICATIONS & USAGE

    - if you put this into your vaginas deeply, it will show its effectsas
    - it melts and soaked into your skin by itself after 30~40 minutes
    - please make sure to check sediments by having a sitz batn
    - your wombs will get back to healthy of twenties if you continue to use one pill per 2~3days


  • WARNINGS

    - please do not use it during the period or if you are pregnant
    - store avoid direct sunlight, high temperatures, and humidity
    - keep in a cool and dry place
  • DOSAGE & ADMINISTRATION

    - women that the lower abdoment or the hands and feet are cold
    - women who have period pain and menstrual irregularity or have a light or heavy flow during your period
    - women that have serious vaginal discharge
    - women who try to prevent urinary incontinence
    - women who feel that their vaginal muscle is relaxed after delivery
  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    LETOMINT 
    clove tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76255-2001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLOVE (UNII: K48IKT5321) (CLOVE - UNII:K48IKT5321) CLOVE18 mg
    Inactive Ingredients
    Ingredient NameStrength
    ALUMINUM SULFATE (UNII: 34S289N54E)  
    GARLIC (UNII: V1V998DC17)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE (UNII: V5VD430YW9)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (ivory white) Scoreno score
    ShapeOVAL (tablet) Size10mm
    FlavorImprint Code 3;hp;x
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76255-2001-118 in 1 BOX
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/18/2011
    Labeler - H&C 21 America Inc (968313267)
    Registrant - H&C 21 America Inc (968313267)
    Establishment
    NameAddressID/FEIBusiness Operations
    GM Manufacturing Inc102301749manufacture