Label: COUGH HP- arsenicum album, bryonia (alba), corallium rubrum, cuprum aceticum, drosera (rotundifolia), ipecacuanha, kali carbonicum, phosphorus, pulsatilla (pratensis), spongia tosta liquid

  • 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 February 12, 2018

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

  • ACTIVE INGREDIENTS:

    Arsenicum Album 30X, Bryonia (Alba) 30X, Corallium Rubrum 30X, Cuprum Aceticum 30X, Drosera (Rotundifolia) 30X, Ipecacuanha 30X, Kali Carbonicum 30X, Phosphorus 30X, Pulsatilla (Pratensis) 30X, Spongia Tosta 30X.

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  • INDICATIONS:

    May temporarily relieve symptoms associated with chronic chest congestion, irritation, tickling, and cough with smarting in the chest.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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  • WARNINGS:

    If pregnant or breastfeeding, ask a health professional before use.

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

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

    Store in a cool, dry place.

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  • 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.

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  • DIRECTIONS:

    Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

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  • INDICATIONS:

    May temporarily relieve symptoms associated with chronic chest congestion, irritation, tickling, and cough with smarting in the chest.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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  • INACTIVE INGREDIENTS:

    Demineralized water, 20% Ethanol.

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  • QUESTIONS:

    Dist. by Energique, Inc.

    201 Apple Blvd.

    Woodbine, IA 51579   800.868.8078

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  • PACKAGE LABEL DISPLAY:

    ENERGIQUE
    SINCE 1987
    HOMEOPATHIC REMEDY
    COUGH HP
    1 fl. oz. (30 ml)

    Cough HP

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  • INGREDIENTS AND APPEARANCE
    COUGH  HP
    arsenicum album, bryonia (alba), corallium rubrum, cuprum aceticum, drosera (rotundifolia), ipecacuanha, kali carbonicum, phosphorus, pulsatilla (pratensis), spongia tosta liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0319
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 30 [hp_X]  in 1 mL
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 30 [hp_X]  in 1 mL
    CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (CORALLIUM RUBRUM EXOSKELETON - UNII:2CA71K0DLE) CORALLIUM RUBRUM EXOSKELETON 30 [hp_X]  in 1 mL
    CUPRIC ACETATE (UNII: 39M11XPH03) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC ACETATE 30 [hp_X]  in 1 mL
    DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA 30 [hp_X]  in 1 mL
    IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC 30 [hp_X]  in 1 mL
    POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 30 [hp_X]  in 1 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 30 [hp_X]  in 1 mL
    ANEMONE PRATENSIS (UNII: 8E272251DI) (ANEMONE PRATENSIS - UNII:8E272251DI) ANEMONE PRATENSIS 30 [hp_X]  in 1 mL
    SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED 30 [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:44911-0319-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 01/12/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/12/2016
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(44911-0319) , api manufacture(44911-0319) , label(44911-0319) , pack(44911-0319)
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