sulphur
Generic: sulfur
Labeler: boironDrug Facts
Product Profile
Brand Name
sulphur
Generic Name
sulfur
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
sulfur 10 [hp_M]/10[hp_M]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-4821
Product ID
0220-4821_0a33fb78-6d1d-3344-e063-6394a90a1861
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
02204821
Hyphenated Format
0220-4821
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
- 10 [hp_M]/10[hp_M]
Packaging
- 10 [hp_M] in 1 TUBE (0220-4821-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a33fb78-6d1d-3344-e063-6394a90a1861", "openfda": {"unii": ["70FD1KFU70"], "spl_set_id": ["8696c9d6-22eb-4eb7-e053-2991aa0abd54"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 [hp_M] in 1 TUBE (0220-4821-41)", "package_ndc": "0220-4821-41", "marketing_start_date": "19830303"}], "brand_name": "Sulphur", "product_id": "0220-4821_0a33fb78-6d1d-3344-e063-6394a90a1861", "dosage_form": "PELLET", "product_ndc": "0220-4821", "generic_name": "SULFUR", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulphur", "active_ingredients": [{"name": "SULFUR", "strength": "10 [hp_M]/10[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}