kali iodatum
Generic: potassium iodide
Labeler: boironDrug Facts
Product Profile
Brand Name
kali iodatum
Generic Name
potassium iodide
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
potassium iodide 6 [hp_X]/1
Manufacturer
Identifiers & Regulatory
Product NDC
0220-2887
Product ID
0220-2887_0a0e1540-968e-93c6-e063-6294a90a6e77
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
1983-03-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02202887
Hyphenated Format
0220-2887
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
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 iodatum (source: ndc)
Generic Name
potassium iodide (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 [hp_X]/1
Packaging
- 80 PELLET in 1 TUBE (0220-2887-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0e1540-968e-93c6-e063-6294a90a6e77", "openfda": {"unii": ["1C4QK22F9J"], "spl_set_id": ["0725b880-7bd2-11e6-bb67-424c58303031"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PELLET in 1 TUBE (0220-2887-41)", "package_ndc": "0220-2887-41", "marketing_start_date": "19830303"}], "brand_name": "Kali iodatum", "product_id": "0220-2887_0a0e1540-968e-93c6-e063-6294a90a6e77", "dosage_form": "PELLET", "product_ndc": "0220-2887", "generic_name": "POTASSIUM IODIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali iodatum", "active_ingredients": [{"name": "POTASSIUM IODIDE", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}