Graphites

UNIISPL

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

Identification

ManufacturerBoiron

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220236541
30 [hp_C] in 1 TUBE (0220-2365-41)

Annotations

UNII (FDA Substance ID)

4QQN74LH4O

GRAPHITE

RxCUI 90249

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4QQN74LH4O",
    "rxcui": "90249",
    "inchikey": null,
    "display_name": "GRAPHITE",
    "substance_type": "polymer",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9ca4d6aa-e183-4400-b1e0-363cb26209aa": {
      "match": "brand_token",
      "title": "GRAPHITES COMBINATION 9225 (GRAPHITES COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "0220-2365_f2f632f1-0775-47d0-e053-2995a90a8d99",
  "productndc": "0220-2365",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "GRAPHITE",
  "proprietary_name": "Graphites",
  "active_ingred_unit": "[hp_C]/30[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "GRAPHITE",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "30"
}

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