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Abropernol (Heel Inc)

Available Formats

Dosage Form Package Information Links
TABLET 30000 mg in 1 BOTTLE (50114-6134-2) Label Information

Complete Abropernol Information

  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medications out of the reach of children.
  • INDICATIONS AND USAGE

    For the temporary relief of:
    • Dermatitus
    • Minor skin irritations
    • Eczema, hyperhidrosis
    • Hyperkeratosis



  • WARNINGS

    If symptoms persist or worsen, a physician should be consulted. As with any drug, if you are pregnant or nursing a baby, seek the advise of a health care professional before using this product.
  • DOSAGE AND ADMINISTRATION

    Adults and children above 6 years: 1 tablet sublingually or dissolved completely in mouth 3 times daily or as directed by a physician.
    Infants and children to 6 years: 1/2 the adult dosage.

  • ACTIVE INGREDIENT

    Each 300mg tablet contains as active ingredients: Abrotanum 4X, Pulsatilla 4X, Calcarea fluorica 12X 60 mg each; Hamamelis virginiana 4X, Agaricus muscarius 5X, Nitricum acidum 6X, Petroleum 6X 30 mg each.

  • INACTIVE INGREDIENT

    Inactive ingredients: Lactose, Magnesium Stearate

  • PURPOSE

    Dermatitus, Minor skin irritations, Eczema, hyperhidrosis, Hyperkeratosis
  • INGREDIENTS AND APPEARANCE
    ABROPERNOL 
    artemisia abrotanum flowering top and pulsatilla vulgaris and calcium fluoride and hamamelis virginiana root bark/stem bark and amanita muscaria var. muscaria fruiting body and nitric acid and kerosene tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:50114-6134
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0) (ARTEMISIA ABROTANUM FLOWERING TOP - UNII:QG07G580U0) ARTEMISIA ABROTANUM FLOWERING TOP 4 [hp_X]  in 300 mg
    PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 4 [hp_X]  in 300 mg
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (CALCIUM FLUORIDE - UNII:O3B55K4YKI) CALCIUM FLUORIDE 12 [hp_X]  in 300 mg
    HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 4 [hp_X]  in 300 mg
    AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY - UNII:DIF093I037) AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY 5 [hp_X]  in 300 mg
    NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4) NITRIC ACID 6 [hp_X]  in 300 mg
    KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 6 [hp_X]  in 300 mg
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    Color white Score no score
    Shape ROUND (Tablet) Size 9mm
    Flavor Imprint Code Heel
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:50114-6134-2 30000 mg in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/31/1984
    Labeler - Heel Inc (102783016)
    Establishment
    Name Address ID/FEI Business Operations
    Heel Inc 102783016 manufacture