graphitis
Generic: graphitis
Labeler: true botanica, llcDrug Facts
Product Profile
Brand Name
graphitis
Generic Name
graphitis
Labeler
true botanica, llc
Dosage Form
GLOBULE
Routes
Active Ingredients
graphite 30 [hp_X]/23g
Manufacturer
Identifiers & Regulatory
Product NDC
53645-1670
Product ID
53645-1670_faa4bfea-4b7c-e530-e053-6294a90a5e5f
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
2014-02-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
536451670
Hyphenated Format
53645-1670
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
graphitis (source: ndc)
Generic Name
graphitis (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 [hp_X]/23g
Packaging
- 23 g in 1 BOTTLE (53645-1670-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "faa4bfea-4b7c-e530-e053-6294a90a5e5f", "openfda": {"unii": ["4QQN74LH4O"], "spl_set_id": ["61952fe1-813f-ff6e-e053-2a91aa0a2d58"], "manufacturer_name": ["True Botanica, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "23 g in 1 BOTTLE (53645-1670-2)", "package_ndc": "53645-1670-2", "marketing_start_date": "20140203"}], "brand_name": "Graphitis", "product_id": "53645-1670_faa4bfea-4b7c-e530-e053-6294a90a5e5f", "dosage_form": "GLOBULE", "product_ndc": "53645-1670", "generic_name": "Graphitis", "labeler_name": "True Botanica, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Graphitis", "active_ingredients": [{"name": "GRAPHITE", "strength": "30 [hp_X]/23g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20140203", "listing_expiration_date": "20261231"}