NDC 43857-0052

DHEA Forte

Dehydroepiandrosterone (dhea), Pregnenolone, Progesterone,

DHEA Forte is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioactive Nutritionals, Inc.. The primary component is Prasterone; Pregnenolone; Progesterone.

• Product ID: 43857-0052_22cd0355-dccf-41af-993e-2b8e6b4ccfea
• NDC: 43857-0052
• Product Type: Human Otc Drug
• Proprietary Name: DHEA Forte
• Generic Name: Dehydroepiandrosterone (dhea), Pregnenolone, Progesterone,
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2012-08-07
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: BioActive Nutritionals, Inc.
• Substance Name: PRASTERONE; PREGNENOLONE; PROGESTERONE
• Active Ingredient Strength: 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 43857-0052-1

30 mL in 1 BOTTLE, SPRAY (43857-0052-1)

• Marketing Start Date: 2016-03-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43857-0052-1 [43857005201]

DHEA Forte LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-03-15

Drug Details

Active Ingredients

Ingredient	Strength
PRASTERONE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 663affc1-0998-4231-b284-ff3e2a7807b9
• Manufacturer:
  • BioActive Nutritionals, Inc.
• UNII:
  • 73R90F7MQ8
  • 459AG36T1B
  • 4G7DS2Q64Y