NUX VOMICA PELLET [HOMEOLAB USA INC]

NUX VOMICA PELLET [HOMEOLAB USA INC]
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NDC 60512-1035-1
Set ID 17485071-4cf9-4013-9443-9669e9e6d1c7
Category HUMAN OTC DRUG LABEL
Packager HOMEOLAB USA INC
Generic Name
Product Class
Product Number
Application Number
  • ACTIVE INGREDIENT HPUS

    NUX VOMICA 3X

    (Quaker buttons)

  • PURPOSE

    STOMACH DISORDERS

  • USE

    For self-limiting condition listed above or as directed by a health professional.

  • WARNINGS

    Enter section text here

    Do not use if pellet-dispenser seal is broken.

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

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

    Keep out of reach of children.

  • DIRECTIONS

    (Adults / Children 2-18 years): Allow 3 or 4 pellets to dissolve in the mouth 3 times a day until symptoms are relieved or as directed by a health professional.

  • OTHER INFORMATION

    Store at room temperature.

  • INACTIVE INGREDIENTS

    Lactose, sucrose.

  • QUESTIONS?

    1-800-404-4666

  • REFERENCES

    The letters HPUS indicate the ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

  • DESCRIPTION

    80 Pellets

    Pellet dispenser

    HOMEOLAB USA INC., 3025 De L`Assomption, Montreal, QC, H1N 2H2, CANADA

    Product of Canada

  • LABEL

    image of tube label

  • INGREDIENTS AND APPEARANCE
    NUX VOMICA 
    nux vomica pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60512-1035
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED3 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    SUCROSE (UNII: C151H8M554)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60512-1035-180 in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/11/1995
    Labeler - HOMEOLAB USA INC (202032533)
    Establishment
    NameAddressID/FEIBusiness Operations
    HOMEOLAB USA INC202032533manufacture

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