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Arnica Montana 200C HPUS

NDC 80004-200, Arnica Montana, tablet, from VITAMEDICA, INC..

Product NDC
80004-200
Status
Listed
Labeler
VITAMEDICA, INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED HOMEOPATHIC
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80004-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ARNICA MONTANA WHOLE200 [hp_C]/1
Package NDCNDC-11Package
80004-200-10800040200101 BOTTLE in 1 CARTON (80004-200-10) / 150 TABLET in 1 BOTTLE
80004-200-20800040200201 BLISTER PACK in 1 CARTON (80004-200-20) / 30 TABLET in 1 BLISTER PACK

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 80004-200 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80004-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80004-200. 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.