NDC 43853-0035

TestoPRO

Avena Sativa, Damiana, Hamamelis Virginiana, Korean Ginseng, Populus Tremuloides, Baryta Carbonica, Hepar Suis, Nuphar Luteum, Orchitinum Suis, Phosphoricum Acidum, Sabal Serulata, Selenium Metallicum, Testosterone, Tribulus Terrestris, Horny Goat Weed, Tongkat Ali, Fenugreek

TestoPRO is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Problen. The primary component is Avena Sativa Flowering Top; Turnera Diffusa Leafy Twig; Hamamelis Virginiana Root Bark/stem Bark; Asian Ginseng; Populus Tremuloides Whole; Barium Carbonate; Pork Liver; Nuphar Lutea Root; Sus Scrofa Testicle; Phosphoric Acid; Saw Palmetto; Selenium; Testosterone; Tribulus Terrestris Whole; Epimedium Grandiflorum Top; Eurycoma Longifolia Whole; Fenugreek Seed.

Product ID43853-0035_26055f9b-afb4-4d71-b57a-42bef7792671
NDC43853-0035
Product TypeHuman Otc Drug
Proprietary NameTestoPRO
Generic NameAvena Sativa, Damiana, Hamamelis Virginiana, Korean Ginseng, Populus Tremuloides, Baryta Carbonica, Hepar Suis, Nuphar Luteum, Orchitinum Suis, Phosphoricum Acidum, Sabal Serulata, Selenium Metallicum, Testosterone, Tribulus Terrestris, Horny Goat Weed, Tongkat Ali, Fenugreek
Dosage FormSpray
Route of AdministrationORAL
Marketing Start Date2017-06-28
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameProBlen
Substance NameAVENA SATIVA FLOWERING TOP; TURNERA DIFFUSA LEAFY TWIG; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; ASIAN GINSENG; POPULUS TREMULOIDES WHOLE; BARIUM CARBONATE; PORK LIVER; NUPHAR LUTEA ROOT; SUS SCROFA TESTICLE; PHOSPHORIC ACID; SAW PALMETTO; SELENIUM; TESTOSTERONE; TRIBULUS TERRESTRIS WHOLE; EPIMEDIUM GRANDIFLORUM TOP; EURYCOMA LONGIFOLIA WHOLE; FENUGREEK SEED
Active Ingredient Strength1 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
DEA ScheduleCIII
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 43853-0035-1

30 mL in 1 BOTTLE (43853-0035-1)
Marketing Start Date2017-06-28
NDC Exclude FlagN
Sample Package?N

Drug Details


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