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NDC 24794-102, Sodium Fluoride, gel, from Crosstex International Inc..

Product NDC
24794-102
Status
Listed
Labeler
Crosstex International 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/24794-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5.6 g/454g
Package NDCNDC-11Package
24794-102-1624794010216454 g in 1 BOTTLE, PLASTIC (24794-102-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/49ca4fc7-6f1a-47e7-9d0c-d015c9a3c202

Use it

Look up 24794-102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24794-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24794-102. 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.