Package 0220-2871-41

Brand: kali chloricum

Generic: potassium chlorate
NDC Package

Package Facts

Identity

Package NDC 0220-2871-41
Digits Only 0220287141
Product NDC 0220-2871
Description

30 [hp_C] in 1 TUBE (0220-2871-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand kali chloricum
Generic potassium chlorate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0e1efd-9eb7-83d7-e063-6294a90a9643", "openfda": {"unii": ["H35KS68EE7"], "spl_set_id": ["7cab8360-b7c7-ad11-e053-2991aa0a3cc1"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-2871-41)", "package_ndc": "0220-2871-41", "marketing_start_date": "19830303"}], "brand_name": "Kali chloricum", "product_id": "0220-2871_0a0e1efd-9eb7-83d7-e063-6294a90a9643", "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": "0220-2871", "generic_name": "POTASSIUM CHLORATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali chloricum", "active_ingredients": [{"name": "POTASSIUM CHLORATE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}