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Indole (Deseret Biologicals, Inc.)

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LIQUID 30 mL in 1 BOTTLE, DROPPER (43742-0212-1) Label Information

Complete Indole Information

  • ACTIVE INGREDIENTS

    Indolum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C


  • INDICATIONS

    For temporary relief of bowel disorders as with colitis, celiac disease, improper digestion, and flatulence, allergies caused by pollens or foods including gluten intolerance, and/or nasal and sinus congestion, candidiasis, sleep disorders and depression. 


  • WARNINGS

    Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

    If pregnant or breast-feeding, seek advice of a health professional before use.

    Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.


  • DIRECTIONS

    1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.


  • INACTIVE INGREDIENTS

    Demineralized water, 25% Ethanol.


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.


  • INDICATIONS AND USAGE

    For temporary relief of bowel disorders as with colitis, celiac disease, improper digestion, and flatulence, allergies caused by pollens or foods including gluten intolerance, and/or nasal and sinus congestion, candidiasis, sleep disorders and depression.


  • QUESTIONS

    Dist. By: Deseret Biologicals, Inc.

    469 Parkland Drive

    Sandy, UT 84070

    www.desbio.com


  • PACKAGE LABEL DISPLAY

    DESBIO
    NDC 43742-0212-1
    HOMEOPATHIC
    INDOLE
    1 FL OZ (30 ml)

    Indole


  • INGREDIENTS AND APPEARANCE
    INDOLE 
    indolum liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0212
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    INDOLE (UNII: 8724FJW4M5) (INDOLE - UNII:8724FJW4M5) INDOLE 6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43742-0212-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 04/03/2013 08/24/2020
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 04/03/2013 08/24/2020
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(43742-0212) , api manufacture(43742-0212) , label(43742-0212) , pack(43742-0212)