Label: CARDIOPAR (convallaria majalis, apocynum cannabinum, arteria suis, heart (suis), thyroidinum- suis, adonis vernalis, cactus grandiflorus, digitalis purpurea, lycopus virginicus 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 June 8, 2023

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

  • ACTIVE INGREDIENTS:

    (in each drop): 12.49% of Adonis Vernalis 10X, Arteria Suis 8X, Cactus Grandiflorus 12X, Convallaria Majalis 4X, Digitalis Purpurea 12X, Heart (Suis) 8X, Lycopus Virginicus 12X, Thyroidinum (Suis) 8X; 0.10% of Apocynum Cannabinum 6X.

  • INDICATIONS:

    May temporarily relieve difficulty breathing after walking, tiredness, feeling as if you can't breathe, and profuse perspiration.**

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

  • 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.

  • 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.

  • DIRECTIONS:

    Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

  • INDICATIONS:

    May temporarily relieve difficulty breathing after walking, tiredness, feeling as if you can't breathe, and profuse perspiration.**

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

  • INACTIVE INGREDIENTS:

    Demineralized water, 20% Ethanol.

  • QUESTIONS:

    Dist. by Energique, Inc.
    201 Apple Blvd.
    Woodbine, IA 51579 800.869.8078

  • PACKAGE LABEL DISPLAY:

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

    Cardiopar

  • INGREDIENTS AND APPEARANCE
    CARDIOPAR 
    convallaria majalis, apocynum cannabinum, arteria suis, heart (suis), thyroidinum (suis), adonis vernalis, cactus grandiflorus, digitalis purpurea, lycopus virginicus liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0532
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CONVALLARIA MAJALIS (UNII: QHH4HVF5QE) (CONVALLARIA MAJALIS - UNII:QHH4HVF5QE) CONVALLARIA MAJALIS4 [hp_X]  in 1 mL
    APOCYNUM CANNABINUM ROOT (UNII: 2F92409L9Z) (APOCYNUM CANNABINUM ROOT - UNII:2F92409L9Z) APOCYNUM CANNABINUM ROOT6 [hp_X]  in 1 mL
    SUS SCROFA ARTERY (UNII: 63O327782Q) (SUS SCROFA ARTERY - UNII:63O327782Q) SUS SCROFA ARTERY8 [hp_X]  in 1 mL
    PORK HEART (UNII: X876KJM95L) (PORK HEART - UNII:X876KJM95L) PORK HEART8 [hp_X]  in 1 mL
    THYROID (UNII: 6RV024OAUQ) (THYROID - UNII:6RV024OAUQ) THYROID8 [hp_X]  in 1 mL
    ADONIS VERNALIS WHOLE (UNII: DX3ZNI25WK) (ADONIS VERNALIS WHOLE - UNII:DX3ZNI25WK) ADONIS VERNALIS WHOLE10 [hp_X]  in 1 mL
    SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (SELENICEREUS GRANDIFLORUS STEM - UNII:7114SV0MYK) SELENICEREUS GRANDIFLORUS STEM12 [hp_X]  in 1 mL
    DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS12 [hp_X]  in 1 mL
    LYCOPUS VIRGINICUS WHOLE (UNII: TWH5125Q6F) (LYCOPUS VIRGINICUS WHOLE - UNII:TWH5125Q6F) LYCOPUS VIRGINICUS WHOLE12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0532-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product02/26/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic02/26/2020
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(44911-0532) , api manufacture(44911-0532) , label(44911-0532) , pack(44911-0532)