Package 0220-3745-41
Brand: ocimum canum
Generic: ocimum americanum leafPackage Facts
Identity
Package NDC
0220-3745-41
Digits Only
0220374541
Product NDC
0220-3745
Description
200 [kp_C] in 1 TUBE (0220-3745-41)
Marketing
Marketing Status
Brand
ocimum canum
Generic
ocimum americanum leaf
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a9d9aa0-dbf4-4241-e063-6294a90a8b51", "openfda": {"unii": ["4EX119B76E"], "spl_set_id": ["3a9d9aa0-dbf3-4241-e063-6294a90a8b51"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-3745-41)", "package_ndc": "0220-3745-41", "marketing_start_date": "20250101"}], "brand_name": "OCIMUM CANUM", "product_id": "0220-3745_3a9d9aa0-dbf4-4241-e063-6294a90a8b51", "dosage_form": "PELLET", "product_ndc": "0220-3745", "generic_name": "OCIMUM AMERICANUM LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OCIMUM CANUM", "active_ingredients": [{"name": "OCIMUM AMERICANUM LEAF", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}