Label: NATRUM SULPHURICUM- sodium sulfate tablet, chewable

  • NDC Code(s): 60512-8032-5, 60512-8032-6
  • Packager: HOMEOLAB USA INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

Drug Label Information

Updated 03/14

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  • Active ingredients HPUS

    Natrum sulphuricum (Sodium sulphate) 12X

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  • Purpose

    ...........................................Nausea, vomiting, flatulent diarrhea

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  • REFERENCES

    The letters 'HPUS' indicate that the component in this product is officially monographed in the Homoeopathic Pharmacopoeia of the United States.

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  • Uses

    This tissue salt helps relieve symptoms of nausea, vomiting and flatulent diarrhea.*

    *These claims have not been reviewed by the Food and Drug Administration. They are based on traditional homeopathic practice.

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  • Warnings

    Stop use and ask a doctor if symptoms persist for more than 7 days or worsen.

    As with any drug, ask a doctor before use if pregnant or nursing.

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

    In case of emergency or accidental overdose, contact a medical professional or a Poison Control Center immediately.

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  • Directions

    Children from 2 to 5 years: Crush 2 tablets and dissolve in water 3 times daily, or as directed by a healthcare professional.

    Adults and children over 5 years: Chew 2 tablets 3 times daily, or as directed by a healthcare professional.


    • Do not use more than directed.

    • Do not take with food.

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  • Other information

    Store at room temperature.

    Do not use if cap seal is broken or missing.

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  • Inactive ingredients

    Lactose, magnesium stearate.

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  • LABEL
  • INGREDIENTS AND APPEARANCE
    NATRUM SULPHURICUM 
    natrum sulphuricum tablet, chewable
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-8032
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE 12 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    Color white Score no score
    Shape ROUND Size 8mm
    Flavor Imprint Code NONE
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:60512-8032-5 125 in 1 JAR
    2 NDC:60512-8032-6 500 in 1 JAR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 03/25/2014
    Labeler - HOMEOLAB USA INC (202032533)
    Establishment
    Name Address ID/FEI Business Operations
    HOMEOLAB USA INC 202032533 manufacture(60512-8032)
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