Natrum Muriaticum by Ratis, LLC NATRUM MURIATICUM spray

Natrum Muriaticum by

Drug Labeling and Warnings

Natrum Muriaticum by is a Homeopathic medication manufactured, distributed, or labeled by Ratis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

INGREDIENTS AND APPEARANCE

NATRUM MURIATICUM 
natrum muriaticum spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71753-8009
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	6 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71753-8009-1	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/30/2020	10/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/30/2020	10/26/2025

Labeler - Ratis, LLC (964594324)