Package 0220-3838-41
Brand: oxalicum acidum
Generic: oxalic acid dihydratePackage Facts
Identity
Package NDC
0220-3838-41
Digits Only
0220383841
Product NDC
0220-3838
Description
200 [kp_C] in 1 TUBE (0220-3838-41)
Marketing
Marketing Status
Brand
oxalicum acidum
Generic
oxalic acid dihydrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a9d4e84-118f-0eca-e063-6294a90a73cc", "openfda": {"unii": ["0K2L2IJ59O"], "spl_set_id": ["3a9d4e84-118e-0eca-e063-6294a90a73cc"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-3838-41)", "package_ndc": "0220-3838-41", "marketing_start_date": "20250101"}], "brand_name": "OXALICUM ACIDUM", "product_id": "0220-3838_3a9d4e84-118f-0eca-e063-6294a90a73cc", "dosage_form": "PELLET", "product_ndc": "0220-3838", "generic_name": "OXALIC ACID DIHYDRATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OXALICUM ACIDUM", "active_ingredients": [{"name": "OXALIC ACID DIHYDRATE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}