- Product NDC
- 17089-290
- 11-digit product format
- 170890290
- Labeler code
- 17089
- Product ID
- 17089-290_7e9133b3-3360-2bd0-e053-2a91aa0a3bf3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ARSENIC TRIOXIDE - ESTRADIOL - GOLDENSEAL - LACHESIS MUTA VENOM - MAGNESIUM PHOSPHATE - MATRICARIA RECUTITA - MELATONIN - PROGESTERONE - STRYCHNOS NUX-VOMICA SEED - SULFUR - SUS SCROFA OVARY - SUS SCROFA PITUITARY GLAND -
- Dosage form
- SOLUTION/ DROPS
- Route
- ORAL
- Labeler
- Guna spa
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2006-05-23
- Substance
- ARSENIC TRIOXIDE; ESTRADIOL; GOLDENSEAL; LACHESIS MUTA VENOM; MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE; MATRICARIA RECUTITA; MELATONIN; PROGESTERONE; STRYCHNOS NUX-VOMICA SEED; SULFUR; SUS SCROFA OVARY; SUS SCROFA PITUITARY GLAND
- Active strength
- 6; 6; 6; 4; 6; 6; 4; 6; 6; 6; 8; 8 [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL
- Pharmacologic classes
- Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Progesterone [CS], Progesterone [EPC], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes