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DHEA Forte
DHEA Forte - 43857-0052-1 - (Dehydroepiandrosterone (DHEA), Pregnenolone, Progesterone,)
Drug Information of DHEA Forte
| Product NDC: | 43857-0052 |
| Proprietary Name: | DHEA Forte |
| Non Proprietary Name: | Dehydroepiandrosterone (DHEA), Pregnenolone, Progesterone, |
| Active Ingredient(s): | 6; 6; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Dehydroepiandrosterone (DHEA), Pregnenolone, Progesterone, |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DHEA Forte
| Product NDC: | 43857-0052 |
| Labeler Name: | BioActive Nutritionals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120807 |
Package Information of DHEA Forte
| Package NDC: | 43857-0052-1 |
| Package Description: | 30 mL in 1 BOTTLE, SPRAY (43857-0052-1) |
NDC Information of DHEA Forte
| NDC Code | 43857-0052-1 |
| Proprietary Name | DHEA Forte |
| Package Description | 30 mL in 1 BOTTLE, SPRAY (43857-0052-1) |
| Product NDC | 43857-0052 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dehydroepiandrosterone (DHEA), Pregnenolone, Progesterone, |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120807 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | BioActive Nutritionals, Inc. |
| Substance Name | PRASTERONE; PREGNENOLONE; PROGESTERONE |
| Strength Number | 6; 6; 6 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes |
