52796-177 NDC - 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)

Drug Information

  • Product NDC: 52796-177
  • Proprietary Name: Floriva
  • Non Proprietary Name: 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
  • Active Ingredient(s): 20 [iU]/1 .ALPHA.-TOCOPHEROL; 75 mg/1 ASCORBIC ACID; 1000 [iU]/1 BETA CAROTENE; 40 ug/1 BIOTIN; 600 [iU]/1 CHOLECALCIFEROL; 1 mg/1 CUPRIC OXIDE; 6 ug/1 CYANOCOBALAMIN; 100 ug/1 FOLIC ACID; 162 ug/1 LEVOMEFOLATE GLUCOSAMINE; 15 mg/1 NIACINAMIDE; 1.8 mg/1 PYRIDOXINE; 1.5 mg/1 RIBOFLAVIN; 1 mg/1 SODIUM FLUORIDE; 1.3 mg/1 THIAMINE; 1000 [iU]/1 VITAMIN A ACETATE; 5 mg/1 ZINC GLUCONATE
  • Administration Route(s): ORAL
  • Dosage Form(s): TABLET, CHEWABLE
  • Pharmacy Class(es): Analogs/Derivatives [Chemical/Ingredient]; Ascorbic Acid [CS]; Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]; Vitamin A [CS]; Vitamin A [EPC]; Vitamin B 12 [CS]; Vitamin B 6 [Chemical/Ingredient]; Vitamin B12 [EPC]; Vitamin B6 Analog [EPC]; Vitamin C [EPC]; Vitamin D [CS]; Vitamin D [EPC]

Labeler Information

Field Name Field Value
Labeler Name: BonGeo Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:10/15/2014

Package Information

No. Package Code Package Description Billing Unit
152796-177-9090 TABLET, CHEWABLE in 1 BOTTLE (52796-177-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC52796-177The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEFlorivaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEVITAMIN 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 FLUORIDEThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLET, CHEWABLEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE10/15/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEBonGeo Pharmaceuticals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME.ALPHA.-TOCOPHEROL; ASCORBIC ACID; BETA CAROTENE; BIOTIN; CHOLECALCIFEROL; CUPRIC OXIDE; CYANOCOBALAMIN; FOLIC ACID; LEVOMEFOLATE GLUCOSAMINE; NIACINAMIDE; PYRIDOXINE; RIBOFLAVIN; SODIUM FLUORIDE; THIAMINE; VITAMIN A ACETATE; ZINC GLUCONATEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH20; 75; 1000; 40; 600; 1; 6; 100; 162; 15; 1.8; 1.5; 1; 1.3; 1000; 5 
ACTIVE INGRED UNIT[iU]/1; mg/1; [iU]/1; ug/1; [iU]/1; mg/1; ug/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; mg/1 
PHARM CLASSESAnalogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Vitamin A [CS], Vitamin A [EPC], Vitamin B 12 [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B12 [EPC], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC] 

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This page was last updated on: 12/6/2025

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