absinthium
Generic: wormwood
Labeler: boironDrug Facts
Product Profile
Brand Name
absinthium
Generic Name
wormwood
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
wormwood 30 [hp_C]/30[hp_C]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-0018
Product ID
0220-0018_ff987d6c-5941-9a21-e053-6394a90a41b7
Product Type
HUMAN PRESCRIPTION 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
02200018
Hyphenated Format
0220-0018
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
absinthium (source: ndc)
Generic Name
wormwood (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 [hp_C]/30[hp_C]
Packaging
- 30 [hp_C] in 1 TUBE (0220-0018-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ff987d6c-5941-9a21-e053-6394a90a41b7", "openfda": {"unii": ["F84709P2XV"], "spl_set_id": ["687ce6db-8fea-289f-e053-2a91aa0ae916"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0018-41)", "package_ndc": "0220-0018-41", "marketing_start_date": "19830303"}], "brand_name": "Absinthium", "product_id": "0220-0018_ff987d6c-5941-9a21-e053-6394a90a41b7", "dosage_form": "PELLET", "product_ndc": "0220-0018", "generic_name": "WORMWOOD", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Absinthium", "active_ingredients": [{"name": "WORMWOOD", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}