Drug Information

Product NDC: 43857-0052

Proprietary Name: DHEA Forte

Non Proprietary Name: Dehydroepiandrosterone (DHEA), Pregnenolone, Progesterone,

Active Ingredient(s):
  • 6 [hp_X]/mL PRASTERONE;
  • 6 [hp_X]/mL PREGNENOLONE;
  • 6 [hp_X]/mL PROGESTERONE

Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Progesterone [CS];
  • Progesterone [EPC]

Labeler Information

Labeler Name: BioActive Nutritionals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Start Marketing Date:8/7/2012

Package Information

No. Package Code Package Description Billing Unit
143857-0052-130 mL in 1 BOTTLE, SPRAY (43857-0052-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43857-0052The 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 OTC 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 NAMEDHEA ForteThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEDehydroepiandrosterone (DHEA), Pregnenolone, Progesterone,The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe 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 DATE8/7/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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 NAMEBioActive Nutritionals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEPRASTERONE; PREGNENOLONE; PROGESTERONEAn 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 INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESProgesterone [CS], Progesterone [EPC] 

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This page was last updated on: 5/3/2024