Package 0220-2393-41
Brand: hekla lava
Generic: hekla lavaPackage Facts
Identity
Package NDC
0220-2393-41
Digits Only
0220239341
Product NDC
0220-2393
Description
12 [hp_C] in 1 TUBE (0220-2393-41)
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": "f9117281-c432-c08d-e053-6294a90af4eb", "openfda": {"unii": ["C21158IIRK"], "spl_set_id": ["85b4f8db-bdc1-12d0-e053-2a91aa0a8c5b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 [hp_C] in 1 TUBE (0220-2393-41)", "package_ndc": "0220-2393-41", "marketing_start_date": "19830303"}], "brand_name": "Hekla lava", "product_id": "0220-2393_f9117281-c432-c08d-e053-6294a90af4eb", "dosage_form": "PELLET", "product_ndc": "0220-2393", "generic_name": "HEKLA LAVA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hekla lava", "active_ingredients": [{"name": "HEKLA LAVA", "strength": "12 [hp_C]/12[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}