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NDC 24794-101, Sodium Fluoride, gel, from Crosstex International Inc..

Product NDC
24794-101
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/24794-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5.6 g/454g
Package NDCNDC-11Package
24794-101-1624794010116454 g in 1 BOTTLE, PLASTIC (24794-101-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0da6a9de-ad38-4c75-8e88-b68dfc638edc

Use it

Look up 24794-101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24794-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24794-101. 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.