Label: SCHUESSLER TISSUE SALTS NAT MUR FLUID BALANCE 9- natrum muriaticum tablet, chewable
- NDC Code(s): 84999-021-01
- Packager: Martin & Pleasance Pty Ltd
- 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 August 4, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients Purpose
- PURPOSE
- Uses
-
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
If pregnant or breastfeeding: Ask a health professional before use.
Ask a doctor before use if you have:
• Fever get worse or lasts more than 3 days
• Symptoms persist for more than 7 days or worsen
• Inflammation or inflection is present or develops.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: Chew 1 tablet every 30 minutes until symptoms subside up to 6 times per day.
Maintenance dose: Chew 1 tablet, 4 times daily.
Children 6 years and older: Acute dose: Crush 1/2 tablet, dissolve in water, and take every 30 minutes until symptoms subside, up to six times per day.
Maintenance dose :Crush 1/2 tablet, dissolve in water, 4 times per day.
- Other Information
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- Product label
-
INGREDIENTS AND APPEARANCE
SCHUESSLER TISSUE SALTS NAT MUR FLUID BALANCE 9
natrum muriaticum tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84999-021 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] Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) Product Characteristics Color white Score no score Shape OVAL Size 12mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84999-021-01 1 in 1 CARTON 07/01/2025 1 125 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/01/2025 Labeler - Martin & Pleasance Pty Ltd (752869859)
