graphites
Generic: graphite
Labeler: boironDrug Facts
Product Profile
Brand Name
graphites
Generic Name
graphite
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
graphite 9 [hp_C]/9[hp_C]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-2362
Product ID
0220-2362_0a0b1f9e-167b-1b36-e063-6394a90abcac
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
02202362
Hyphenated Format
0220-2362
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
graphites (source: ndc)
Generic Name
graphite (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 9 [hp_C]/9[hp_C]
Packaging
- 9 [hp_C] in 1 TUBE (0220-2362-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0b1f9e-167b-1b36-e063-6394a90abcac", "openfda": {"unii": ["4QQN74LH4O"], "spl_set_id": ["85a564a9-a628-fda0-e053-2a91aa0adaf0"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-2362-41)", "package_ndc": "0220-2362-41", "marketing_start_date": "19830303"}], "brand_name": "Graphites", "product_id": "0220-2362_0a0b1f9e-167b-1b36-e063-6394a90abcac", "dosage_form": "PELLET", "product_ndc": "0220-2362", "generic_name": "GRAPHITE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Graphites", "active_ingredients": [{"name": "GRAPHITE", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}