Formica rufa

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
0220214041
200 [kp_C] in 1 TUBE (0220-2140-41)

Annotations

UNII (FDA Substance ID)

55H0W83JO5

FORMICA RUFA

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "55H0W83JO5",
    "rxcui": null,
    "inchikey": null,
    "display_name": "FORMICA RUFA",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "285fbafd-f390-49df-e063-6394a90a42c9": {
      "match": "brand_token",
      "title": "FORMICA APIS LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "2",
      "published_date": "2025-12-10"
    }
  },
  "productid": "0220-2140_0a0cd0a0-f2ca-c28b-e063-6394a90ac393",
  "productndc": "0220-2140",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FORMICA RUFA",
  "proprietary_name": "Formica rufa",
  "active_ingred_unit": "[kp_C]/200[kp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "FORMICA RUFA",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "200"
}

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