- Product NDC
- 50181-0023
- 11-digit product format
- 501810023
- Labeler code
- 50181
- Product ID
- 50181-0023_5e239647-8b72-47cb-9471-bd5e28b211ce
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Estriol, Estradiol, Folliculinum, Belladonna, Chelidonium Majus, Hydrocortisone, Glandula Suprarenalis Suis, Hypothalamus suis, Oophorinum suis, Pineal suis, Pituitary suis, Sanguinaria Canadensis, Lilium Tigrinum, Pulsatilla, Sepia, Sulphur
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center for Research and Education
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-04-04
- Marketing end
- 0000-00-00
- Substance
- ESTRIOL; ESTRADIOL; ESTRONE; ATROPA BELLADONNA WHOLE; CHELIDONIUM MAJUS; HYDROCORTISONE; SUS SCROFA ADRENAL GLAND; SUS SCROFA HYPOTHALAMUS; SUS SCROFA OVARY; SUS SCROFA PINEAL GLAND; SUS SCROFA PITUITARY GLAND; SANGUINARIA CANADENSIS ROOT; LILIUM LANCIFOLIUM WHOLE FLOWERING; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; SULFUR
- Active strength
- 6 [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; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record