Package 0220-2392-41
Brand: hekla lava
Generic: hekla lavaPackage Facts
Identity
Package NDC
0220-2392-41
Digits Only
0220239241
Product NDC
0220-2392
Description
9 [hp_C] in 1 TUBE (0220-2392-41)
Marketing
Marketing Status
Brand
hekla lava
Generic
hekla lava
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0d797d-0084-5811-e063-6394a90a4d82", "openfda": {"unii": ["C21158IIRK"], "spl_set_id": ["85b4f8db-bd47-12d0-e053-2a91aa0a8c5b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-2392-41)", "package_ndc": "0220-2392-41", "marketing_start_date": "19830303"}], "brand_name": "Hekla lava", "product_id": "0220-2392_0a0d797d-0084-5811-e063-6394a90a4d82", "dosage_form": "PELLET", "product_ndc": "0220-2392", "generic_name": "HEKLA LAVA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hekla lava", "active_ingredients": [{"name": "HEKLA LAVA", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}