SCHUESSLER TISSUE SALTS NAT SULPH WATER ELIMINATOR 11- natrum sulphuricum spray

Schuessler Tissue Salts Nat Sulph Water Eliminator 11 by

Drug Labeling and Warnings

Schuessler Tissue Salts Nat Sulph Water Eliminator 11 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 Sulphuricum 6X HPUS                                      poor digestion, liver upsets, mild water retention

PURPOSE

Uses

Temporarily relieves symptoms associated with:

Poor digestion

Liver upsets

Mild water retention

Warnings

Stop use and ask a doctor if:

• Symptoms persist for more than 72 hours or worsen 
• New symptoms occur 
• Upper abdominal pain, nausea, loss of appetite, fatigue and malaise if present should be discussed with a doctor 
• If urine is dark in color or stools are pale in color, consult a doctor
• Itchy skin with no visible rash should be investigated by a doctor 
• If water retention causes swelling or edema, consult with a doctor. If water retention is severe, or persists for more than 24 hours consult a doctor.

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 SULPH WATER ELIMINATOR 11 
natrum sulphuricum spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84999-011
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM SULFATE ANHYDROUS	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: 84999-011-01	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)