Package 0220-0187-41

Brand: aloe

Generic: aloe ferox leaf
NDC Package

Package Facts

Identity

Package NDC 0220-0187-41
Digits Only 0220018741
Product NDC 0220-0187
Description

30 [hp_C] in 1 TUBE (0220-0187-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand aloe
Generic aloe ferox leaf
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f7e5e7e2-efb8-6c9e-e053-6394a90aaa7c", "openfda": {"unii": ["0D145J8EME"], "spl_set_id": ["83eca9cb-ce49-2c9c-e053-2a91aa0a80b7"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0187-41)", "package_ndc": "0220-0187-41", "marketing_start_date": "19830303"}], "brand_name": "Aloe", "product_id": "0220-0187_f7e5e7e2-efb8-6c9e-e053-6394a90aaa7c", "dosage_form": "PELLET", "product_ndc": "0220-0187", "generic_name": "ALOE FEROX LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aloe", "active_ingredients": [{"name": "ALOE FEROX LEAF", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}