Label: MOTION SICKNESS- anamirta cocculus seed - strychnos nux-vomica seed - kerosene pellet

  • NDC Code(s): 68428-024-14
  • Packager: Washington Homeopathic Products
  • 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 December 28, 2015

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  • ACTIVE INGREDIENTS

    COCCULUS    6C

    NUX VOM   6C

    PETROLEUM       6C

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  • USES

    To relieve the symptoms of traveling sickness from any cause.  Characterized by dizziness, intense nausea, vomiting.

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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:

    COCCULUS    Motion sickness

    NUX VOM   Vomiting

    PETROLEUM     Nausea

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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 2 pellets every 3 hours for 2 days. Then 2 pellets morning and night for 2 weeks.

    Children: 1 pellet. Repeat as necessary.

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  • INACTIVE INGREDIENTS

    Sucrose/Lactose

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  • PRINCIPAL DISPLAY PANEL

    image of bottle labelEnter section text here

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  • INGREDIENTS AND APPEARANCE
    MOTION SICKNESS 
    anamirta cocculus seed - strychnos nux-vomica seed - kerosene pellet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68428-024
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 6 [hp_C]  in 28 g
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 6 [hp_C]  in 28 g
    KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 6 [hp_C]  in 28 g
    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:68428-024-14 28 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 05/05/2010
    Labeler - Washington Homeopathic Products (084929389)
    Establishment
    Name Address ID/FEI Business Operations
    Washington Homeopathic Products 084929389 manufacture(68428-024)
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