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Arnica Power

NDC 61096-1032, Arnica montana, liquid, from Eight and Company L.L.C.

Product NDC
61096-1032
Status
Listed
Labeler
Eight and Company L.L.C
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/61096-1032 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ARNICA MONTANA WHOLE3 [hp_X]/41mL
Package NDCNDC-11Package
61096-1032-1610961032011 BOTTLE, SPRAY in 1 CARTON (61096-1032-1) / 41 mL in 1 BOTTLE, SPRAY

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 61096-1032 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/61096-1032 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 61096-1032. 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.