Label: ACONITE NAPELLIS- aconitum napellus root tablet

  • 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 28, 2017

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  • ACTIVE INGREDIENT

    ACONITUM NAPELLUS 30X

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  • PURPOSE

    SUDDEN COLDS OR FEVERS

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  • INDICATIONS & USAGE

    SUDDEN COLDS OR FEVERS

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  • Directions

    Adults: Dissolve 4 tablets under tongue 4 times a day. Children: 2 tablets as above.

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  • INACTIVE INGREDIENT

    In a base of Acacia Gum and Lactose N.F.

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  • Warnings

    Do not use if cap band is missing or broken.

    If you are pregnant or nursing, consult a licensed health care professional before using this product.

    If symptoms persist for 7 days or worsen, contact a licensed practitioner.

    Keep this and all medicines out of the reach of children.

    To be used according to label indications and/or standard homeopathic indications.

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  • Questions?

    800-624-9659

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  • PRINCIPAL DISPLAY PANEL - 250 Tablet Bottle Label

    SINCE 1903

    Hyland's®

    HOMEOPATHIC

    NDC 54973-2900-4

    Homeopathic Medicine

    ACONITUM

    NAPELLUS

    30X

    SUDDEN COLDS OR FEVERS

    250 TABLETS

    Label

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  • INGREDIENTS AND APPEARANCE
    ACONITE NAPELLIS 
    aconitum napellus root tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-2900
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACONITUM NAPELLUS ROOT (UNII: KPD2N7348X) (ACONITUM NAPELLUS ROOT - UNII:KPD2N7348X) ACONITUM NAPELLUS ROOT 30 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    ACACIA (UNII: 5C5403N26O)  
    LACTOSE (UNII: J2B2A4N98G)  
    Product Characteristics
    Color brown Score no score
    Shape ROUND Size 9mm
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:54973-2900-4 250 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/1955
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/01/1955
    Labeler - Hyland's (028570695)
    Establishment
    Name Address ID/FEI Business Operations
    Standard Homeopathic Company 008316655 manufacture(54973-2900) , pack(54973-2900)
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