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NDC 60258-151, 1.1% Sodium Fluoride, gel, from Cypress Pharmaceutical, Inc..

Product NDC
60258-151
Status
Listed
Labeler
Cypress Pharmaceutical, Inc.
Dosage form
GEL
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/60258-151 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE11 mg/g
Package NDCNDC-11Package
60258-151-01602580151011 TUBE in 1 CARTON (60258-151-01) / 56 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b7c0a768-7e8a-40b9-876f-b86d3dc5e848

Use it

Look up 60258-151 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60258-151 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60258-151. 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.