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NUX VOMICA

NDC 15631-2868, NUX VOMICA, liquid, from Rxhomeo Private Limited d.b.a. Rxhomeo, Inc.

Product NDC
15631-2868
Status
Listed
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, 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/15631-2868 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • STRYCHNOS NUX-VOMICA SEED3 [hp_X]/mL

Pharmacologic classes

Allergens [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Seed Storage Proteins [CS]

Package NDCNDC-11Package
15631-2868-01563128680010 mL in 1 BOTTLE (15631-2868-0)
15631-2868-11563128680130 mL in 1 BOTTLE (15631-2868-1)

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 15631-2868 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/15631-2868 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 15631-2868. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.