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Schuessler Tissue Salts Nat Sulph Water Eliminator 11

NDC 84999-023 · Martin & Pleasance Pty Ltd

Generic nameNatrum Sulphuricum
Dosage formTABLET, CHEWABLE
RouteORAL
Active ingredient(s)SODIUM SULFATE ANHYDROUS
Strength6 [hp_X]/1
Pharmacologic classIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

84999-023-01 — 1 BOTTLE in 1 CARTON (84999-023-01) / 125 TABLET, CHEWABLE in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10572-100 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 24338-236 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 40032-090 — POLYETHYLENE GLYCOL-3350 AND ELECTROLYTES, 43386-060 — polyethylene glycol-3350 and electrolytes with Flavor Pack, 43386-090 — polyethylene glycol-3350 and Electrolytes, 50090-6521 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 50090-8020 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 51672-4170 — sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate, 52268-100 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 52536-236 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 54973-6440 — sodium sulfate anhydrous, 58264-0341 — COLCHICUM AUTUMNALE WHOLE, SODIUM SULFATE ANHYDROUS, and NAJA NAJA WHOLE, 64380-765 — Polyethylene Glycol 3350 and electrolytes - Unflavored, 64380-766 — Polyethylene Glycol 3350 and electrolytes with Lemon Flavor, 64380-767 — Polyethylene Glycol 3350 and electrolytes with Orange Flavor, 84999-011 — Natrum Sulphuricum

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels