Label: DIARALIA- arsenic trioxide,cinchona officinalis bark, podophyllum tablet

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

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated May 10, 2023

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

  • ACTIVE INGREDIENT

    Active ingredients** (in each tablet)

    Arsenicum album 9C HPUS (0.83 mg)

    Cinchona officinalis 5C HPUS (0.83 mg)

    Podophyllum peltatum 9C HPUS (0.83 mg)

    The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

  • INDICATIONS & USAGE

    Uses*

    temporarily relieves symptoms of diarrhea such as:

    • traveler's diarrhea
    • intestinal pain
    • bloating
    • gas
    • nausea
    • vomiting

  • PURPOSE

    Purpose*

    Arsenicum album 9C HPUS (0.83 mg) ... Relieves diarrhea with nausea, vomiting, and weakness. (contains less that 10 -18 mg arsenic)

    Cinchona officinalis 5C HPUS (0.83 mg) ... Relieves diarrhea with gas and bloating

    Podophyllum peltatum 9C HPUS (0.83 mg) ... Relieves diarrhea with intestinal rumbling and pain

  • WARNINGS

  • ASK DOCTOR

    Ask a doctor before use if you have

    fever

    bloody or black stool

    mucus in your stool.

  • STOP USE

    Stop use and ask a doctor if symptoms persist for more than 2 days or worsen.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Drink plenty of clear fluids to help prevent dehydration caused by diarrhea.

    • Adults and children 6 years of age and older: At the onset of symptoms, dissolve 2 tablets in the mouth every 4 to 6 hours, up to 2 days maximum. Discontinue use as soon as symptoms disappear.
    • Children under 6 years of age: Ask a doctor.
  • SPL UNCLASSIFIED SECTION

    do not use if glued carton end flaps are open or if the blister seal is broken.

    store below 86° F (30° C)

    60 Meltaway Tablets

    No Known Drug Interactions

    Diarrhea Relief*

    Intestinal Pain Nausea Traveler's Diarrhea*

    *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
    *C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

  • INACTIVE INGREDIENT

    lactose, croscarmellose sodium, magnesium stearate

  • QUESTIONS

    1-800-BOIRON-1 (1-800-264-7661),
    BoironUSA.com Info@boiron.com
    Distributed by Boiron, Inc. Newtown Square, PA 19073

  • PRINCIPAL DISPLAY PANEL

    labellabellabel6891220image

  • INGREDIENTS AND APPEARANCE
    DIARALIA 
    arsenic trioxide,cinchona officinalis bark, podophyllum tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0220-9095
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PODOPHYLLUM (UNII: 2S713A4VP3) (PODOPHYLLUM - UNII:2S713A4VP3) PODOPHYLLUM9 [hp_C]
    CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB) CINCHONA OFFICINALIS BARK5 [hp_C]
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE9 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize9mm
    FlavorImprint Code Boiron
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0220-9095-0460 in 1 CARTON08/01/2019
    160 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/01/2019
    Labeler - BOIRON (282560473)
    Registrant - BOIRON, INC. (014892269)
    Establishment
    NameAddressID/FEIBusiness Operations
    BOIRON282560473manufacture(0220-9095)