Label: NATRUM SULPHURICUM spray

  • 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 January 20, 2022

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENT:

    Natrum Sulphuricum 6X.

  • USES:

    Helps relieve nausea, vomiting, bitter taste, diarrhea, and influenza. Eliminates toxins and supports liver health.**

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

  • WARNINGS:

    For oral use only.

    If pregnant or breast-feeding, or if symptoms persist or worsen, ask a health care professional.

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

    Do not use if tamper evident seal is broken or missing.

  • KEEP OUT OF REACH OF CHILDREN:

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS:

    Adults: 2 sprays 3 times a day or as needed.

    Children 2-12: 1 spray as above. For children 12 and under, consult a doctor.

  • INDICATIONS:

    Helps relieve nausea, vomiting, bitter taste, diarrhea, and influenza. Eliminates toxins and supports liver health.**

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

  • INACTIVE INGREDIENTS:

    Demineralized Water, Organic Ethanol 20%

  • QUESTIONS:

    Comments? Visit

    HomeopathyStore.com

    or call (888) 405-7551.

    Distributed by:

    Ratis, LLC,

    211 E. Lombard St, STE 303,

    Baltimore, MD 21202

  • PACKAGE LABEL DISPLAY:

    NDC 71753-8011-1

    LACTOSE FREE

    Anna's

    REMEDIES

    NATRUM SULPHURICUM

    HOMEOPATHIC ORAL SPRAY

    1 FL. OZ (30ML)

    NATRUM SULPHURICUM

  • INGREDIENTS AND APPEARANCE
    NATRUM SULPHURICUM 
    natrum sulphuricum spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71753-8011
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71753-8011-130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/30/202010/26/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/30/202010/26/2025
    Labeler - Ratis, LLC (964594324)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!