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Menopause

NDC 50845-0092, Agnus Castus, Angelica Sinensis Radix, Apis Mellifica, Aralia Quinquefolia, Arnica Montana, Cimicifuga Racemosa, Galium Aparine, Glycyrrhiza Glabra, Oophorinum Suis, Sepia, Thuja Occidentalis, Viscum Album, liquid, from Liddell Laboratories, Inc..

Product NDC
50845-0092
Status
Listed
Labeler
Liddell Laboratories, Inc.
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/50845-0092 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHASTE TREE3 [hp_X]/mL
  • ANGELICA SINENSIS ROOT3 [hp_X]/mL
  • APIS MELLIFERA6 [hp_X]/mL
  • AMERICAN GINSENG3 [hp_X]/mL
  • ARNICA MONTANA WHOLE6 [hp_X]/mL
  • BLACK COHOSH3 [hp_X]/mL
  • GALIUM APARINE WHOLE3 [hp_X]/mL
  • GLYCYRRHIZA GLABRA3 [hp_X]/mL
  • SUS SCROFA OVARY30 [hp_C]/mL
  • SEPIA OFFICINALIS JUICE30 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG6 [hp_X]/mL
  • VISCUM ALBUM FRUITING TOP3 [hp_X]/mL

Pharmacologic classes

Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Standardized Insect Venom Allergenic Extract [EPC]

Package NDCNDC-11Package
50845-0092-2508450092021 BOTTLE, SPRAY in 1 CARTON (50845-0092-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0092-1)

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 50845-0092 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50845-0092 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50845-0092. 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.