Label: BRONCHIAL COUGH THERAPY- antimony potassium tartrate - protortonia cacti - drosera rotundifolia - echinacea, unspecified - calcium sulfide - human sputum, bordetella pertussis infected - spongia officinalis skeleton, roasted - tablet, orally disintegrating

  • 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 November 17, 2018

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

  • ACTIVE INGREDIENT

    Active IngredientsPurpose
    Antimonium tartaricum HPUS6c, 12c, 18cRattling cough
    Coccus cacti HPUS6c, 12c, 18cCongestive cough
    Drosera HPUS6c, 12c, 18cDry tickling cough
    Echinacea HPUS6c, 12c, 18cImmune system support
    Hepar sulphuris calcareum HPUS6c, 12c, 18cExpectorant
    Pertussinum HPUS18cRecurring and Spasmodic coughing attacks
    Spongia tosta HPUS6c, 12c, 18cDry barking cough

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

  • PURPOSE

  • Uses

    According to homeopathic indications these ingredients provide temporary relief of symptoms of Bronchial Cough such as: • coughing • mucous build-up • chest tightness and • chest soreness after diagnosis by a physician.

  • Warnings

    USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN.

    • This product is a not a fast acting (rescue) inhaler.
    • This product is intended to complement, not replace, standard medical treatment.
    • Initial worsening of symptoms may occur.
    • A physician should always be consulted to rule out serious causes.
    • In case of overdose, get medical help or contact a Poison Control Center right away.

    Stop use and ask a doctor if:

    • You experience worsening symptoms.
    • If symptoms last longer than 7 days.

  • Keep out of reach of children

  • PREGNANCY OR BREAST FEEDING

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

  • Directions

    • Suitable for adults and children 12 years and above.
    • Dissolve entire tablet under tongue.
    • Do not chew or swallow whole.
    • Take 1 tablet 3 times a day or as directed by a physician.
    • Use up to 6 times a day as needed.
    • Take at least 10 minutes before or at least 10 minutes after eating or drinking.
    • Children under the age of 12: consult a physician before use.
  • Other information

    • Active ingredients are micro-diluted in accordance with the Homeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects.
    • Store in a cool dark location.
  • Inactive Ingredients

    Advantol® 300, Lactose, Magnesium Stearate, Mannitol, Microcrystalline Cellulose.

  • Do not use if tamper evident seal is torn, broken or missing.

  • QUESTIONS

    For more information and to order related products call toll free: 888-969-6855 or trpcompany.com

  • PRINCIPAL DISPLAY PANEL

    Bottle image

    Box image


  • INGREDIENTS AND APPEARANCE
    BRONCHIAL COUGH THERAPY 
    antimony potassium tartrate - protortonia cacti - drosera rotundifolia - echinacea, unspecified - calcium sulfide - human sputum, bordetella pertussis infected - spongia officinalis skeleton, roasted - tablet, orally disintegrating
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17312-018
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE6 [hp_C]
    PROTORTONIA CACTI (UNII: LZB7TFX1LT) (PROTORTONIA CACTI - UNII:LZB7TFX1LT) PROTORTONIA CACTI6 [hp_C]
    DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA6 [hp_C]
    ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX) ECHINACEA, UNSPECIFIED6 [hp_C]
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE6 [hp_C]
    HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN) (HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - UNII:U364V64HUN) HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED18 [hp_C]
    SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED6 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    MANNITOL (UNII: 3OWL53L36A)  
    SORBITOL (UNII: 506T60A25R)  
    CROSPOVIDONE (UNII: 2S7830E561)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    COPOVIDONE (UNII: D9C330MD8B)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeDIAMONDSize13mm
    FlavorImprint Code TRP
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17312-018-141 in 1 PACKAGE12/01/2011
    170 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic12/01/2011
    Labeler - TRP Company (105185719)
    Registrant - TRP Company (105185719)