Prostate
- Product NDC
- 43742-0469
- 11-digit product format
- 437420469
- Labeler code
- 43742
- Product ID
- 43742-0469_ce9245fd-399c-4263-a0a2-77ec42af950b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Petroselinum Sativum, Populus Tremulodies, Sabal Serrulata, Chimaphila Umbellata, Adenosinum Triphosphoricum Dinatrum, Equol, Kreosotum, Nadidum, Testosterone, Succinicum Acidum, Hepar Sulphuris Calcareum, Prostate Nosode, Conium Maculatum, Proteus (Mirabilis), Proteus (Vulgaris)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-03-20
- Marketing end
- 2020-05-20
- Substance
- PETROSELINUM CRISPUM; POPULUS TREMULOIDES BARK; POPULUS TREMULOIDES LEAF; SAW PALMETTO; CHIMAPHILA UMBELLATA; ADENOSINE TRIPHOSPHATE DISODIUM; EQUOL, (+/-)-; WOOD CREOSOTE; NADIDE; TESTOSTERONE; SUCCINIC ACID; CALCIUM SULFIDE; SUS SCROFA PROSTATE; CONIUM MACULATUM FLOWERING TOP; PROTEUS MIRABILIS; PROTEUS VULGARIS
- Active strength
- 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record