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Pro-Den Rx

NDC 59883-911, Sodium Fluoride, rinse, from Den-Mat Holdings, Llc.

Product NDC
59883-911
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/59883-911 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE9 mg/mL
Package NDCNDC-11Package
59883-911-64598830911641890 mL in 1 BOTTLE, PLASTIC (59883-911-64)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ba020e07-ad41-4419-a503-f1245131b7d2

Use it

Look up 59883-911 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59883-911 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59883-911. 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.