NUX VOMICA (STRYCHNOS NUX-VOMICA SEED ) PELLET [BOIRON]

NUX VOMICA (STRYCHNOS NUX-VOMICA SEED ) PELLET [BOIRON]
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NDC 0220-3707-41
Set ID 865a27ab-6ba6-aef5-e053-2a91aa0a1f72
Category HUMAN OTC DRUG LABEL
Packager Boiron
Generic Name
Product Class
Product Number
Application Number
  • ACTIVE INGREDIENT

    Nux vomica 200CK

    (**contains 0.443 mg of the active ingredient per pellet)

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  • INDICATIONS & USAGE

    Heartburn Or Drowsiness Due To Excessive Eating Or Drinking*

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  • STOP USE

    Stop use and ask a doctor if symptoms persist for more than 3 days or worsen

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  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding ask a health professional before use

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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  • SPL UNCLASSIFIED SECTION

    Do not use if pellet dispenser seal is broken.
    Contains approx 80 pellets.
    How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue.
    *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
    *C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

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  • INACTIVE INGREDIENT

    lactose, sucrose

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  • DOSAGE & ADMINISTRATION

    Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

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  • QUESTIONS

    1-800-BOIRON-1 (1-800-264-7661),
    BoironUSA.com Info@boiron.com
    Distributed by Boiron, Inc. Newtown Square, PA 19073

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  • INGREDIENTS AND APPEARANCE
    NUX VOMICA 
    strychnos nux-vomica seed pellet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-3707
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 200 [kp_C]  in 200 [kp_C]
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    Product Characteristics
    Color white Score     
    Shape ROUND Size 4mm
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0220-3707-41 200 [kp_C] in 1 TUBE; Type 0: Not a Combination Product 03/03/1983
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 03/03/1983
    Labeler - Boiron (282560473)
    Registrant - Boiron, Inc. (014892269)
    Establishment
    Name Address ID/FEI Business Operations
    Boiron 282560473 manufacture(0220-3707)
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