SCHUESSLER TISSUE SALTS NAT MUR FLUID BALANCE 9- natrum muriaticum spray

Schuessler Tissue Salts Nat Mur Fluid Balance 9 by

Drug Labeling and Warnings

Schuessler Tissue Salts Nat Mur Fluid Balance 9 by is a Homeopathic medication manufactured, distributed, or labeled by Martin & Pleasance Pty Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient (in each spray)                              Purpose

Natrum Muriaticum 6X HPUS                                     excessive moisture, nasal discharge,watery eyes, dryness of the lips, skin or eyes

“ HPUS” is the Homeopathic Pharmacopoeia of the United States                                            

PURPOSE

Uses

Temporarily relieves symptoms associated with:

• Excessive moisture 
• Nasal discharge
• Watery eyes
• Dryness of the lips, skin or eyes.

Warnings

Stop use and ask a doctor if:

• Symptoms persist for more than 72 hours or worsen 
• New symptoms occur 
• Redness or swelling is present
• Nasal congestion worsens or sinusitis occurs 
• Eyes feel red or itchy
• Skin dryness results in pain or lesions.

Ask a doctor before use if you have: 

• Fever gets worse or lasts more than 3 days 
• Symptoms persist for more than 7 days or worsen 
• Inflammation or infection is present or develops.

If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

Directions

• Use as directed 
• Take 30 minutes away from food.

Adults

• Acute dose: Spray into the mouth 4 times every 30 mins until symptoms subside, up to 8 times per day.
• Maintenance dose: Spray into mouth 4 times, 4 times per day.

Other Information

Store below 86°F

Inactive Ingredients

Alcohol, Glycerin, Purified Water

SPL UNCLASSIFIED SECTION

Questions?www.schuesslertissuesalts.co or + 1-888-464-6775

Product label

INGREDIENTS AND APPEARANCE

SCHUESSLER TISSUE SALTS NAT MUR FLUID BALANCE 9 
natrum muriaticum spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84999-009
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 30 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84999-009-01	1 in 1 CARTON	02/01/2025
1		30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/01/2025

Labeler - Martin & Pleasance Pty Ltd (752869859)