Package 0220-0190-41

Brand: aloe

Generic: aloe ferox leaf
NDC Package

Package Facts

Identity

Package NDC 0220-0190-41
Digits Only 0220019041
Product NDC 0220-0190
Product ID 0220-0190_0051d268-8f32-5d6e-e063-6394a90a01e2
Description

6 [hp_C] in 1 TUBE (0220-0190-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "0051d268-8f32-5d6e-e063-6394a90a01e2", "openfda": {"unii": ["0D145J8EME"], "spl_set_id": ["83ec645b-ae8e-5979-e053-2991aa0a554f"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-0190-41)", "package_ndc": "0220-0190-41", "marketing_start_date": "19830303"}], "brand_name": "Aloe", "product_id": "0220-0190_0051d268-8f32-5d6e-e063-6394a90a01e2", "dosage_form": "PELLET", "product_ndc": "0220-0190", "generic_name": "ALOE FEROX LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aloe", "active_ingredients": [{"name": "ALOE FEROX LEAF", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}