- Product NDC
- 50181-0019
- 11-digit product format
- 501810019
- Labeler code
- 50181
- Product ID
- 50181-0019_ec58a298-7df5-4570-a561-fbafe36b98c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxytocin, Chimaphila Umbellata, Pituitary (Suis), Uva Ursi, Orchitinum (Suis), Prostate (Suis), Sarsaparilla, Gelsemium Sempervirens, Zincum Metallicum, Kali Phosphoricum, Phosphoricum Acidum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center for Research and Education
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-04-08
- Marketing end
- 0000-00-00
- Substance
- OXYTOCIN; CHIMAPHILA UMBELLATA; SUS SCROFA PITUITARY GLAND; ARCTOSTAPHYLOS UVA-URSI LEAF; SUS SCROFA TESTICLE; SUS SCROFA PROSTATE; SARSAPARILLA; GELSEMIUM SEMPERVIRENS ROOT; ZINC; POTASSIUM PHOSPHATE, DIBASIC; PHOSPHORIC ACID
- Active strength
- 6 [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record