52747-621 NDC - CONCEPT DHA (VITAMIN- MINERAL OMEGA-3 SUPPLEMENT)

Drug Information

Product NDC: 52747-621

Proprietary Name: Concept DHA

Non Proprietary Name: Vitamin- Mineral Omega-3 Supplement

Active Ingredient(s):
  • 25 mg/1 ASCORBIC ACID;
  • 300 ug/1 BIOTIN;
  • 5 mg/1 CALCIUM PANTOTHENATE;
  • 2 mg/1 CUPRIC SULFATE;
  • 12.5 ug/1 CYANOCOBALAMIN;
  • 17.5 mg/1 FERROUS FUMARATE;
  • 1 mg/1 FOLIC ACID;
  • 17.5 mg/1 IRON;
  • 5 mg/1 MAGNESIUM SULFATE, UNSPECIFIED FORM;
  • 1.8 mg/1 NIACIN;
  • 200 mg/1 OMEGA-3-ACID ETHYL ESTERS;
  • 25 mg/1 PYRIDOXINE HYDROCHLORIDE;
  • 3 mg/1 RIBOFLAVIN;
  • 2 mg/1 THIAMINE MONONITRATE;
  • 10 mg/1 ZINC SULFATE, UNSPECIFIED FORM


Administration Route(s): ORAL

Dosage Form(s): CAPSULE, LIQUID FILLED

Pharmacy Class(es):
  • Analogs/Derivatives [Chemical/Ingredient];
  • Ascorbic Acid [CS];
  • Calculi Dissolution Agent [EPC];
  • Copper Absorption Inhibitor [EPC];
  • Decreased Copper Ion Absorption [PE];
  • Fatty Acids;
  • Omega-3 [CS];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE];
  • Magnesium Ion Exchange Activity [MoA];
  • Nicotinic Acid [EPC];
  • Nicotinic Acids [CS];
  • Omega-3 Fatty Acid [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE];
  • Vitamin B 12 [CS];
  • Vitamin B 6 [Chemical/Ingredient];
  • Vitamin B12 [EPC];
  • Vitamin B6 Analog [EPC];
  • Vitamin C [EPC]

Labeler Information

Labeler Name: U.S. Pharmaceutical Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:6/24/2009

Package Information

No. Package Code Package Description Billing Unit
152747-621-3030 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (52747-621-30)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC52747-621The 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 NAMEConcept DHAThe 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- Mineral Omega-3 SupplementThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECAPSULE, LIQUID FILLEDThe 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 DATE6/24/2009This 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 NAMEU.S. Pharmaceutical CorporationName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEASCORBIC ACID; BIOTIN; CALCIUM PANTOTHENATE; CUPRIC SULFATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; IRON; MAGNESIUM SULFATE, UNSPECIFIED FORM; NIACIN; OMEGA-3-ACID ETHYL ESTERS; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE; ZINC SULFATE, UNSPECIFIED FORMAn 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 STRENGTH25; 300; 5; 2; 12.5; 17.5; 1; 17.5; 5; 1.8; 200; 25; 3; 2; 10 
ACTIVE INGRED UNITmg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 
PHARM CLASSESAnalogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Calculi Dissolution Agent [EPC], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Fatty Acids, Omega-3 [CS], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Nicotinic Acid [EPC], Nicotinic Acids [CS], Omega-3 Fatty Acid [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin B 12 [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B12 [EPC], Vitamin B6 Analog [EPC], Vitamin C [EPC] 

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This page was last updated on: 2/1/2023