Package 0220-1937-41
Brand: eucalyptus globulus
Generic: eucalyptus globulus leafPackage Facts
Identity
Package NDC
0220-1937-41
Digits Only
0220193741
Product NDC
0220-1937
Description
200 [kp_C] in 1 TUBE (0220-1937-41)
Marketing
Marketing Status
Brand
eucalyptus globulus
Generic
eucalyptus globulus leaf
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "16f13c97-0916-a642-e063-6294a90a209c", "openfda": {"unii": ["S546YLW6E6"], "spl_set_id": ["16f13c97-0915-a642-e063-6294a90a209c"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-1937-41)", "package_ndc": "0220-1937-41", "marketing_start_date": "20240101"}], "brand_name": "Eucalyptus globulus", "product_id": "0220-1937_16f13c97-0916-a642-e063-6294a90a209c", "dosage_form": "PELLET", "product_ndc": "0220-1937", "generic_name": "EUCALYPTUS GLOBULUS LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Eucalyptus globulus", "active_ingredients": [{"name": "EUCALYPTUS GLOBULUS LEAF", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}