Package 0220-0222-41

Brand: aloe

Generic: aloe ferox leaf
NDC Package

Package Facts

Identity

Package NDC 0220-0222-41
Digits Only 0220022241
Product NDC 0220-0222
Product ID 0220-0222_227e9fec-6417-d25b-e063-6394a90a08e2
Description

200 [kp_C] in 1 TUBE (0220-0222-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand aloe
Generic aloe ferox leaf
Sample Package No

Linked Drug Pages (1)

Aloe ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "227e9fec-6417-d25b-e063-6394a90a08e2", "openfda": {"unii": ["0D145J8EME"], "spl_set_id": ["227e9fec-6416-d25b-e063-6394a90a08e2"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0222-41)", "package_ndc": "0220-0222-41", "marketing_start_date": "20240101"}], "brand_name": "Aloe", "product_id": "0220-0222_227e9fec-6417-d25b-e063-6394a90a08e2", "dosage_form": "PELLET", "product_ndc": "0220-0222", "generic_name": "ALOE FEROX LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aloe", "active_ingredients": [{"name": "ALOE FEROX LEAF", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}