Label: CV HP (adonis vernalis, lachesis mutus, lycopus virginicus, valeriana officinalis, aurum metallicum, cactus grandiflorus, digitalis purpurea, natrum muriaticum, phosphorus, pulsatilla- pratensis, 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 October 28, 2021

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

  • ACTIVE INGREDIENTS:

    (in each drop): 10% of Adonis Vernalis 30X, Aurum Metallicum 30C, Cactus Grandiflorus 30C, Digitalis Purpurea 30C, Lachesis Mutus 30X, Lycopus Virginicus 30X, Natrum Muriaticum 30C, Phosphorus 30C, Pulsatilla (Pratensis) 30C, Valeriana Officinalis 30X.

  • INDICATIONS:

    May temporarily relieve constriction of the chest cavity, heart sensitivity, difficulty in breathing, and swelling of the ankles.**

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

  • WARNINGS:

    If pregnant or breast-feeding, 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 constriction of the chest cavity, heart sensitivity, difficulty in breathing, and swelling of the ankles.**

    **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

    CV HP

    1 fl. oz. (30 ml)

    CV HP

  • INGREDIENTS AND APPEARANCE
    CV  HP
    adonis vernalis, lachesis mutus, lycopus virginicus, valeriana officinalis, aurum metallicum, cactus grandiflorus, digitalis purpurea, natrum muriaticum, phosphorus, pulsatilla (pratensis), liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0196
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADONIS VERNALIS (UNII: DX3ZNI25WK) (ADONIS VERNALIS - UNII:DX3ZNI25WK) ADONIS VERNALIS30 [hp_X]  in 1 mL
    LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM30 [hp_X]  in 1 mL
    LYCOPUS VIRGINICUS (UNII: TWH5125Q6F) (LYCOPUS VIRGINICUS - UNII:TWH5125Q6F) LYCOPUS VIRGINICUS30 [hp_X]  in 1 mL
    VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW) VALERIAN30 [hp_X]  in 1 mL
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD30 [hp_C]  in 1 mL
    SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (SELENICEREUS GRANDIFLORUS STEM - UNII:7114SV0MYK) SELENICEREUS GRANDIFLORUS STEM30 [hp_C]  in 1 mL
    DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS30 [hp_C]  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE30 [hp_C]  in 1 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS30 [hp_C]  in 1 mL
    PULSATILLA PRATENSIS (UNII: 8E272251DI) (PULSATILLA PRATENSIS - UNII:8E272251DI) PULSATILLA PRATENSIS30 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0196-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product07/09/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/09/2015
    Labeler - ENERGIQUE, INC. (789886132)
    Registrant - APOTHECA COMPANY (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOTHECA COMPANY844330915manufacture(44911-0196) , api manufacture(44911-0196) , label(44911-0196) , pack(44911-0196)