Floriva

UNIISPLATC A11CC

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

Identification

ManufacturerBonGeo Pharmaceuticals, Inc.

CountryUS (United States)

ATC codeA11CC

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5279617250
1 BOTTLE, DROPPER in 1 BOX (52796-172-50) / 50 mL in 1 BOTTLE, DROPPER

Annotations

UNII (FDA Substance ID)

1C6V77QF41

CHOLECALCIFEROL

RxCUI 2418

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1C6V77QF41",
    "rxcui": "2418",
    "inchikey": "QYSXJUFSXHHAJI-YRZJJWOYSA-N",
    "display_name": "CHOLECALCIFEROL",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3d5fbe3a-a95b-4688-a96e-b34e6e1e868a": {
      "match": "brand_token",
      "title": "FLORIVA (VITAMIN A ACETATE, .BETA.-CAROTENE, ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, LEVOMEFOLATE GLUCOSAMINE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, ZINC GLUCONATE, CUPRIC OXIDE, AND SODIUM FLUORIDE) TABLET, CHEWABLE [BONGEO PHARMACEUTICALS, INC.]",
      "spl_version": "4",
      "published_date": "2024-02-02"
    }
  },
  "productid": "52796-172_b70f7032-674d-4052-84d9-35ee99f33868",
  "productndc": "52796-172",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CHOLECALCIFEROL; SODIUM FLUORIDE",
  "proprietary_name": "Floriva",
  "active_ingred_unit": "[iU]/mL; mg/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "CHOLECALCIFEROL and SODIUM FLUORIDE",
  "start_marketing_date": "20141015",
  "active_numerator_strength": "400; .25"
}

Related drugs

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