aurum muriaticum kalinatum

Generic: potassium tetrachloroaurate dihydrate

Labeler: boiron
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name aurum muriaticum kalinatum
Generic Name potassium tetrachloroaurate dihydrate
Labeler boiron
Dosage Form PELLET
Routes
ORAL
Active Ingredients

potassium tetrachloroaurate dihydrate 9 [hp_C]/9[hp_C]

Manufacturer
Boiron

Identifiers & Regulatory

Product NDC 0220-0644
Product ID 0220-0644_09ac80f8-325d-a443-e063-6394a90a1438
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 1983-03-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02200644
Hyphenated Format 0220-0644

Supplemental Identifiers

UNII
SYJ0T39LVU

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 aurum muriaticum kalinatum (source: ndc)
Generic Name potassium tetrachloroaurate dihydrate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 9 [hp_C]/9[hp_C]
source: ndc
Packaging
  • 9 [hp_C] in 1 TUBE (0220-0644-41)
source: ndc

Packages (1)

Ingredients (1)

potassium tetrachloroaurate dihydrate (9 [hp_C]/9[hp_C])

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09ac80f8-325d-a443-e063-6394a90a1438", "openfda": {"unii": ["SYJ0T39LVU"], "spl_set_id": ["84749c71-5f3c-2dda-e053-2991aa0aed8d"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-0644-41)", "package_ndc": "0220-0644-41", "marketing_start_date": "19830303"}], "brand_name": "Aurum muriaticum kalinatum", "product_id": "0220-0644_09ac80f8-325d-a443-e063-6394a90a1438", "dosage_form": "PELLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0220-0644", "generic_name": "POTASSIUM TETRACHLOROAURATE DIHYDRATE", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aurum muriaticum kalinatum", "active_ingredients": [{"name": "POTASSIUM TETRACHLOROAURATE DIHYDRATE", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}