Label: ALDICOM- aldicom a-hat complex liquid

  • 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 December 27, 2021

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  • ACTIVE INGREDIENT

    ALDICOM A-HAT, lactobacillus

  • INACTIVE INGREDIENT

    fryctiikugisaccgarudem sugar fed honey, glucomannan, pueraria montana var. lobata extract

  • PURPOSE

    Alcohol decomposition

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Take 1ea before and after drinking

  • WARNINGS

    Do not take in excess of the specified dose

  • DOSAGE & ADMINISTRATION

    for oral use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ALDICOM 
    aldicom a-hat complex liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73392-0002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LACTOBACILLUS PLANTARUM (UNII: QFC21096ON) (LACTOBACILLUS PLANTARUM - UNII:QFC21096ON) LACTOBACILLUS PLANTARUM1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    HOVENIA DULCIS WHOLE (UNII: 1DM83BAP2N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73392-0002-175 g in 1 PACKAGE; Type 0: Not a Combination Product10/09/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/09/2019
    Labeler - NAME (694977041)
    Registrant - NAME (694977041)
    Establishment
    NameAddressID/FEIBusiness Operations
    NAME694977041manufacture(73392-0002) , label(73392-0002)