Package 0220-5003-41
Brand: thuja occidentalis
Generic: thuja occidentalis leafy twigPackage Facts
Identity
Package NDC
0220-5003-41
Digits Only
0220500341
Product NDC
0220-5003
Description
6 [hp_C] in 1 TUBE (0220-5003-41)
Marketing
Marketing Status
Brand
thuja occidentalis
Generic
thuja occidentalis leafy twig
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "445e99f1-3c34-e3d8-e063-6394a90a3938", "openfda": {"unii": ["1NT28V9397"], "spl_set_id": ["8641fbcd-0f1c-29e6-e053-2a91aa0a5a82"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-5003-41)", "package_ndc": "0220-5003-41", "marketing_start_date": "19830303"}], "brand_name": "Thuja occidentalis", "product_id": "0220-5003_445e99f1-3c34-e3d8-e063-6394a90a3938", "dosage_form": "PELLET", "product_ndc": "0220-5003", "generic_name": "THUJA OCCIDENTALIS LEAFY TWIG", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thuja occidentalis", "active_ingredients": [{"name": "THUJA OCCIDENTALIS LEAFY TWIG", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}