Label: ACONITUM, RADIX- aconitum napellus root pellet

  • NDC Code(s): 68428-865-03, 68428-865-05, 68428-865-06, 68428-865-11, view more
    68428-865-12
  • Packager: Washington Homeopathic Products
  • Category: HUMAN OTC DRUG LABEL

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 July 13, 2016

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENTS

    ACONITUM, RAD   30C

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  • USES

    To relieve the symptoms of fainting.

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  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medicines out of reach of children.

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  • INDICATIONS

    Indications:

    ACONITUM, RAD   High fever

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  • STOP USE AND ASK DOCTOR

    If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

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  • DIRECTIONS

    Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

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  • INACTIVE INGREDIENTS

    Sucrose/Lactose

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  • PRINCIPAL DISPLAY PANEL

    The OTC potency range of ACONITUM, RAD is 6x–30x, 3c–30c, 200c, 1m, 10m, 50m, and CM.
    Availability is subject to change.

    Aconitum, radix label example

    All WHP single remedies are made to order; thus, the labels are printed on the same label stock as the orders are filled.

    ‘Bottle Size’ and ‘Potency’ vary on the label depending on customer choice.

    Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

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  • INGREDIENTS AND APPEARANCE
    ACONITUM, RADIX 
    aconitum napellus root pellet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68428-865
    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_C]
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Product Characteristics
    Color white (white) Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68428-865-03 75 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/08/2013
    2 NDC:68428-865-05 150 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/08/2013
    3 NDC:68428-865-11 300 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/08/2013
    4 NDC:68428-865-12 600 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/08/2013
    5 NDC:68428-865-06 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/08/2013
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 07/08/2013
    Labeler - Washington Homeopathic Products (084929389)
    Establishment
    Name Address ID/FEI Business Operations
    Washington Homeopathic Products 084929389 manufacture(68428-865)
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