Label: NATRUM MURIATICUM 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.

  • ACTIVE INGREDIENT:

    Natrum Muriaticum 6X.

  • USES:

    Helps relieve conditions with excess water or dryness such as runny or stuffy nose, allergies, headaches, migraines, constipation, slow digestion, watery eyes, and dry mouth.**

    **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 conditions with excess water or dryness such as runny or stuffy nose, allergies, headaches, migraines, constipation, slow digestion, watery eyes, and dry mouth.**

    **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 71753-8009-1

    LACTOSE FREE

    Anna's

    REMEDIES

    Natrum Muriaticum

    HOMEOPATHIC ORAL SPRAY

    1 FL. OZ (30ML)

    Natrum Muriaticum

  • INGREDIENTS AND APPEARANCE
    NATRUM MURIATICUM 
    natrum muriaticum spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71753-8009
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71753-8009-130 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)