Package 0220-5002-41

Brand: thuja occidentalis

Generic: thuja occidentalis leafy twig
NDC Package

Package Facts

Identity

Package NDC 0220-5002-41
Digits Only 0220500241
Product NDC 0220-5002
Description

5 [hp_C] in 1 TUBE (0220-5002-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "445e328f-69bd-8377-e063-6294a90a79b1", "openfda": {"unii": ["1NT28V9397"], "spl_set_id": ["8656aa47-6d88-39a1-e053-2991aa0ac012"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 [hp_C] in 1 TUBE (0220-5002-41)", "package_ndc": "0220-5002-41", "marketing_start_date": "19830303"}], "brand_name": "Thuja occidentalis", "product_id": "0220-5002_445e328f-69bd-8377-e063-6294a90a79b1", "dosage_form": "PELLET", "product_ndc": "0220-5002", "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": "5 [hp_C]/5[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}