Package 71753-8007-1
Brand: kali sulphuricum
Generic: kali sulphuricumPackage Facts
Identity
Package NDC
71753-8007-1
Digits Only
7175380071
Product NDC
71753-8007
Description
30 mL in 1 BOTTLE, SPRAY (71753-8007-1)
Marketing
Marketing Status
Brand
kali sulphuricum
Generic
kali sulphuricum
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "755dd085-e530-4320-a574-299151cc654a", "openfda": {"upc": ["0371753800712"], "unii": ["1K573LC5TV"], "spl_set_id": ["f0061e89-ff0e-452e-9a9c-ee24020b3e88"], "manufacturer_name": ["Ratis, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, SPRAY (71753-8007-1)", "package_ndc": "71753-8007-1", "marketing_start_date": "20200930"}], "brand_name": "Kali Sulphuricum", "product_id": "71753-8007_755dd085-e530-4320-a574-299151cc654a", "dosage_form": "SPRAY", "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": "71753-8007", "generic_name": "Kali Sulphuricum", "labeler_name": "Ratis, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali Sulphuricum", "active_ingredients": [{"name": "POTASSIUM SULFATE", "strength": "6 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20200930", "listing_expiration_date": "20261231"}