phosphorus
Generic: phosphorus
Labeler: boironDrug Facts
Product Profile
Brand Name
phosphorus
Generic Name
phosphorus
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
phosphorus 10 [hp_M]/10[hp_M]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-4019
Product ID
0220-4019_f2f5942b-af82-234c-e053-2a95a90ad689
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
02204019
Hyphenated Format
0220-4019
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
phosphorus (source: ndc)
Generic Name
phosphorus (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 [hp_M]/10[hp_M]
Packaging
- 10 [hp_M] in 1 TUBE (0220-4019-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f2f5942b-af82-234c-e053-2a95a90ad689", "openfda": {"unii": ["27YLU75U4W"], "spl_set_id": ["8694ff4d-b056-2ff7-e053-2991aa0a144e"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 [hp_M] in 1 TUBE (0220-4019-41)", "package_ndc": "0220-4019-41", "marketing_start_date": "19830303"}], "brand_name": "Phosphorus", "product_id": "0220-4019_f2f5942b-af82-234c-e053-2a95a90ad689", "dosage_form": "PELLET", "product_ndc": "0220-4019", "generic_name": "PHOSPHORUS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Phosphorus", "active_ingredients": [{"name": "PHOSPHORUS", "strength": "10 [hp_M]/10[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}