Package 0220-2975-41
Brand: kali sulphuricum
Generic: potassium sulfatePackage Facts
Identity
Package NDC
0220-2975-41
Digits Only
0220297541
Product NDC
0220-2975
Description
12 [hp_C] in 1 TUBE (0220-2975-41)
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": "0a0e1efd-9eb8-83d7-e063-6294a90a9643", "openfda": {"unii": ["1K573LC5TV"], "spl_set_id": ["860adf6e-38c0-17b9-e053-2a91aa0a700e"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 [hp_C] in 1 TUBE (0220-2975-41)", "package_ndc": "0220-2975-41", "marketing_start_date": "19830303"}], "brand_name": "Kali sulphuricum", "product_id": "0220-2975_0a0e1efd-9eb8-83d7-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": "0220-2975", "generic_name": "POTASSIUM SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali sulphuricum", "active_ingredients": [{"name": "POTASSIUM SULFATE", "strength": "12 [hp_C]/12[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}