Package 0220-2872-41

Brand: kali chloricum

Generic: potassium chlorate
NDC Package

Package Facts

Identity

Package NDC 0220-2872-41
Digits Only 0220287241
Product NDC 0220-2872
Product ID 0220-2872_3a880519-b150-1eaf-e063-6294a90aaceb
Description

200 [kp_C] in 1 TUBE (0220-2872-41)

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand kali chloricum
Generic potassium chlorate
Sample Package No

Linked Drug Pages (1)

KALI CHLORICUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a880519-b150-1eaf-e063-6294a90aaceb", "openfda": {"unii": ["H35KS68EE7"], "spl_set_id": ["3a880519-b14f-1eaf-e063-6294a90aaceb"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2872-41)", "package_ndc": "0220-2872-41", "marketing_start_date": "20250101"}], "brand_name": "KALI CHLORICUM", "product_id": "0220-2872_3a880519-b150-1eaf-e063-6294a90aaceb", "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": "0220-2872", "generic_name": "POTASSIUM CHLORATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "KALI CHLORICUM", "active_ingredients": [{"name": "POTASSIUM CHLORATE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}