sulphur
Generic: sulfur
Labeler: boironDrug Facts
Product Profile
Brand Name
sulphur
Generic Name
sulfur
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
sulfur 6 [hp_X]/1
Manufacturer
Identifiers & Regulatory
Product NDC
0220-4823
Product ID
0220-4823_0a33e170-e8ae-25a8-e063-6394a90addf5
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
02204823
Hyphenated Format
0220-4823
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
sulphur (source: ndc)
Generic Name
sulfur (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 [hp_X]/1
Packaging
- 80 PELLET in 1 TUBE (0220-4823-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a33e170-e8ae-25a8-e063-6394a90addf5", "openfda": {"unii": ["70FD1KFU70"], "spl_set_id": ["e205d5d0-7c2b-11e6-87a0-424c58303031"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PELLET in 1 TUBE (0220-4823-41)", "package_ndc": "0220-4823-41", "marketing_start_date": "19830303"}], "brand_name": "Sulphur", "product_id": "0220-4823_0a33e170-e8ae-25a8-e063-6394a90addf5", "dosage_form": "PELLET", "product_ndc": "0220-4823", "generic_name": "SULFUR", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulphur", "active_ingredients": [{"name": "SULFUR", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}