NATRUM MURIATICUM- natrum muriaticum spray 
Ratis, LLC

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.

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Drug Facts:

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

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)

Revised: 1/2022
Document Id: cef70a76-b116-46d0-9d67-6d4cf6fe74b9
Set id: 12cd1ff0-44ba-44a4-8317-6411538020dc
Version: 2
Effective Time: 20220120
 
Ratis, LLC