bellis perennis
Generic: bellis perennis
Labeler: boironDrug Facts
Product Profile
Brand Name
bellis perennis
Generic Name
bellis perennis
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
bellis perennis 1 [hp_M]/[hp_M]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-0734
Product ID
0220-0734_09ba5e8f-735b-2a35-e063-6394a90a98d0
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
1983-03-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02200734
Hyphenated Format
0220-0734
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
bellis perennis (source: ndc)
Generic Name
bellis perennis (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 [hp_M]/[hp_M]
Packaging
- 1 [hp_M] in 1 TUBE (0220-0734-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09ba5e8f-735b-2a35-e063-6394a90a98d0", "openfda": {"unii": ["2HU33I03UY"], "spl_set_id": ["850084c3-1dd2-eb8d-e053-2a91aa0a130b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 [hp_M] in 1 TUBE (0220-0734-41)", "package_ndc": "0220-0734-41", "marketing_start_date": "19830303"}], "brand_name": "Bellis perennis", "product_id": "0220-0734_09ba5e8f-735b-2a35-e063-6394a90a98d0", "dosage_form": "PELLET", "product_ndc": "0220-0734", "generic_name": "BELLIS PERENNIS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bellis perennis", "active_ingredients": [{"name": "BELLIS PERENNIS", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}