EndoPure Pro
- Product NDC
- 50181-0022
- 11-digit product format
- 501810022
- Labeler code
- 50181
- Product ID
- 50181-0022_1559c3b7-7cb0-4e9b-9485-a5b1f2c8deca
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- L Arginine, Pineal, Pituitary, Progesteronium, Belladonna, Chelidonium Majus, Dioscorea Villosa, Folliculinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-01-08
- Marketing end
- 0000-00-00
- Substance
- ARGININE; SUS SCROFA PINEAL GLAND; SUS SCROFA PITUITARY GLAND; PROGESTERONE; ATROPA BELLADONNA WHOLE; CHELIDONIUM MAJUS; DIOSCOREA VILLOSA TUBER; ESTRONE; SUS SCROFA ADRENAL GLAND; SUS SCROFA HYPOTHALAMUS; SUS SCROFA OVARY; LILIUM LANCIFOLIUM WHOLE FLOWERING; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; SULFUR
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#