United States · FDA National Drug Code directory

KALI SULPH

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
54973-5230_f0330ffb-503d-2671-e053-2995a90a8218
Product NDC
54973-5230
Form
TABLET
Composition / generic term
potassium sulfate
Labeler
Hyland's Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
19400101
Source listing expiry
20261231

Source-listed ingredients

  • POTASSIUM SULFATE — 6 [hp_X]/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 500 TABLET in 1 BOTTLE, PLASTIC (54973-5230-1) · 54973-5230-1

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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KALI SULPH — United States | Molindra Medicines