sulphur
Generic: sulfur
Labeler: boironDrug Facts
Product Profile
Brand Name
sulphur
Generic Name
sulfur
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
sulfur 30 [hp_X]/30[hp_X]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-4817
Product ID
0220-4817_003abd8e-d4e1-fc69-e063-6394a90a381f
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
02204817
Hyphenated Format
0220-4817
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
- 30 [hp_X]/30[hp_X]
Packaging
- 30 [hp_X] in 1 TUBE (0220-4817-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "003abd8e-d4e1-fc69-e063-6394a90a381f", "openfda": {"unii": ["70FD1KFU70"], "spl_set_id": ["8695c4fb-437f-91c2-e053-2a91aa0a4e71"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_X] in 1 TUBE (0220-4817-41)", "package_ndc": "0220-4817-41", "marketing_start_date": "19830303"}], "brand_name": "Sulphur", "product_id": "0220-4817_003abd8e-d4e1-fc69-e063-6394a90a381f", "dosage_form": "PELLET", "product_ndc": "0220-4817", "generic_name": "SULFUR", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulphur", "active_ingredients": [{"name": "SULFUR", "strength": "30 [hp_X]/30[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}