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NDC 59883-920, Sodium Fluoride, rinse, from Den-mat Holdings, Llc.

Product NDC
59883-920
Status
Listed
Labeler
Den-mat Holdings, Llc
Dosage form
RINSE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59883-920 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE.9 mg/mL
Package NDCNDC-11Package
59883-920-1659883092016473 mL in 1 BOTTLE, PLASTIC (59883-920-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e39b19f7-2b3e-4c77-9544-623ebad84870

Use it

Look up 59883-920 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59883-920 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59883-920. 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.