Package 0220-2976-41
Brand: kali sulphuricum
Generic: potassium sulfatePackage Facts
Identity
Package NDC
0220-2976-41
Digits Only
0220297641
Product NDC
0220-2976
Description
15 [hp_C] in 1 TUBE (0220-2976-41)
Marketing
Marketing Status
Brand
kali sulphuricum
Generic
potassium sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0e6b08-3f30-b3f7-e063-6394a90ae8e3", "openfda": {"unii": ["1K573LC5TV"], "spl_set_id": ["860b6684-28c8-8927-e053-2991aa0aa323"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 [hp_C] in 1 TUBE (0220-2976-41)", "package_ndc": "0220-2976-41", "marketing_start_date": "19830303"}], "brand_name": "Kali sulphuricum", "product_id": "0220-2976_0a0e6b08-3f30-b3f7-e063-6394a90ae8e3", "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": "0220-2976", "generic_name": "POTASSIUM SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali sulphuricum", "active_ingredients": [{"name": "POTASSIUM SULFATE", "strength": "15 [hp_C]/15[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}