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FLUORIDEX

NDC 59883-020, Sodium Fluoride, paste, dentifrice, from DEN-MAT HOLDINGS, LLC..

Product NDC
59883-020
Status
Listed
Labeler
DEN-MAT HOLDINGS, LLC.
Dosage form
PASTE, DENTIFRICE
Route
DENTAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59883-020 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5 mg/g
Package NDCNDC-11Package
59883-020-04598830020041 TUBE in 1 BOX (59883-020-04) / 112 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6014c330-3698-027c-e053-2a91aa0a64e5

Use it

Look up 59883-020 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59883-020 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59883-020. 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.