NDC 63083-2124

PMS Drops 2124

Pms Drops

PMS Drops 2124 is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Professional Complementary Health Formulas. The primary component is Black Cohosh; Bos Taurus Pituitary Gland, Posterior; Caulophyllum Thalictroides Root; Chaste Tree Fruit; Estrogens, Conjugated; Lachesis Muta Venom; Magnesium Phosphate, Dibasic Trihydrate; Progesterone; Pulsatilla Montana Whole; Sepia Officinalis Juice; Spongia Officinalis Skeleton, Roasted; Thyroid, Unspecified; Viburnum Opulus Bark.

Product ID63083-2124_69d060e1-8f98-4b7c-9499-86cb94014b77
NDC63083-2124
Product TypeHuman Otc Drug
Proprietary NamePMS Drops 2124
Generic NamePms Drops
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1984-08-15
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameProfessional Complementary Health Formulas
Substance NameBLACK COHOSH; BOS TAURUS PITUITARY GLAND, POSTERIOR; CAULOPHYLLUM THALICTROIDES ROOT; CHASTE TREE FRUIT; ESTROGENS, CONJUGATED; LACHESIS MUTA VENOM; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PROGESTERONE; PULSATILLA MONTANA WHOLE; SEPIA OFFICINALIS JUICE; SPONGIA OFFICINALIS SKELETON, ROASTED; THYROID, UNSPECIFIED; VIBURNUM OPULUS BARK
Active Ingredient Strength6 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharm ClassesCalculi Dissolution Agent [EPC], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Estrogens, Conjugated (USP) [CS], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Progesterone [CS], Progesterone [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63083-2124-2

59 mL in 1 BOTTLE, DROPPER (63083-2124-2)
Marketing Start Date1985-08-15
NDC Exclude FlagN
Sample Package?N

Drug Details


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