Graphitis

UNII

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerTrue Botanica, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5364516702
23 g in 1 BOTTLE (53645-1670-2)

Annotations

UNII (FDA Substance ID)

4QQN74LH4O

GRAPHITE

RxCUI 90249

Raw payload (JSON)

{
  "unii": {
    "unii": "4QQN74LH4O",
    "rxcui": "90249",
    "inchikey": null,
    "display_name": "GRAPHITE",
    "substance_type": "polymer",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "53645-1670_faa4bfea-4b7c-e530-e053-6294a90a5e5f",
  "productndc": "53645-1670",
  "dosage_form": "GLOBULE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "GRAPHITE",
  "proprietary_name": "Graphitis",
  "active_ingred_unit": "[hp_X]/23g",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Graphitis",
  "start_marketing_date": "20140203",
  "active_numerator_strength": "30"
}

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