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PMS Drops 2124

NDC 63083-2124, PMS Drops, liquid, from Professional Complementary Health Formulas.

Product NDC
63083-2124
Status
Listed
Labeler
Professional Complementary Health Formulas
Dosage form
LIQUID
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED HOMEOPATHIC
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63083-2124 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHASTE TREE FRUIT3 [hp_X]/59mL
  • CAULOPHYLLUM THALICTROIDES ROOT6 [hp_X]/59mL
  • BLACK COHOSH6 [hp_X]/59mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE6 [hp_X]/59mL
  • BOS TAURUS PITUITARY GLAND, POSTERIOR6 [hp_X]/59mL
  • PULSATILLA MONTANA WHOLE6 [hp_X]/59mL
  • SEPIA OFFICINALIS JUICE6 [hp_X]/59mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED6 [hp_X]/59mL
  • THYROID, UNSPECIFIED6 [hp_X]/59mL
  • VIBURNUM OPULUS BARK6 [hp_X]/59mL
  • LACHESIS MUTA VENOM15 [hp_X]/59mL
  • ESTROGENS, CONJUGATED30 [hp_X]/59mL
  • PROGESTERONE30 [hp_X]/59mL

Pharmacologic classes

Calculi 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]

Package NDCNDC-11Package
63083-2124-26308321240259 mL in 1 BOTTLE, DROPPER (63083-2124-2)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 63083-2124 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63083-2124 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63083-2124. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.