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Rhus Aconitum

NDC 48951-8140, Rhus Aconitum, liquid, from Uriel Pharmacy Inc..

Product NDC
48951-8140
Status
Listed
Labeler
Uriel Pharmacy 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/48951-8140 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GELSEMIUM SEMPERVIRENS ROOT4 [hp_X]/mL
  • PSEUDOGNAPHALIUM LUTEOALBUM LEAF4 [hp_X]/mL
  • ACONITUM NAPELLUS6 [hp_X]/mL
  • ATROPA BELLADONNA6 [hp_X]/mL
  • MANDRAGORA OFFICINARUM ROOT6 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF6 [hp_X]/mL
  • PENOXSULAM10 [hp_X]/mL
Package NDCNDC-11Package
48951-8140-14895181400110 AMPULE in 1 BOX (48951-8140-1) / 1 mL in 1 AMPULE

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 48951-8140 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/48951-8140 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 48951-8140. 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.