kali sulph

Generic: potassium sulfate

Labeler: hyland's inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name kali sulph
Generic Name potassium sulfate
Labeler hyland's inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

potassium sulfate 6 [hp_X]/1

Manufacturer
Hyland's Inc.

Identifiers & Regulatory

Product NDC 54973-5230
Product ID 54973-5230_f0330ffb-503d-2671-e053-2995a90a8218
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 1940-01-01

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 549735230
Hyphenated Format 54973-5230

Supplemental Identifiers

UPC
0354973523012
UNII
1K573LC5TV

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name kali sulph (source: ndc)
Generic Name potassium sulfate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 6 [hp_X]/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE, PLASTIC (54973-5230-1)
source: ndc

Packages (1)

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

Ingredients (1)

potassium sulfate (6 [hp_X]/1)

Linked Drug Pages (1)

KALI SULPH ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f0330ffb-503d-2671-e053-2995a90a8218", "openfda": {"upc": ["0354973523012"], "unii": ["1K573LC5TV"], "spl_set_id": ["c00e31d8-76df-47b1-bafd-36d088395522"], "manufacturer_name": ["Hyland's Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (54973-5230-1)", "package_ndc": "54973-5230-1", "marketing_start_date": "19400101"}], "brand_name": "KALI SULPH", "product_id": "54973-5230_f0330ffb-503d-2671-e053-2995a90a8218", "dosage_form": "TABLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "54973-5230", "generic_name": "potassium sulfate", "labeler_name": "Hyland's Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "KALI SULPH", "active_ingredients": [{"name": "POTASSIUM SULFATE", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19400101", "listing_expiration_date": "20261231"}