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NDC 10866-0685, Topical APF Fluoride Gel, gel, from Pascal Company, Inc..

Product NDC
10866-0685
Status
Listed
Labeler
Pascal Company, Inc.
Dosage form
GEL
Route
BUCCAL, DENTAL, TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10866-0685 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE27.73 mg/g
Package NDCNDC-11Package
10866-0685-210866068502480 g in 1 BOTTLE, PLASTIC (10866-0685-2)

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/1235c694-a139-4d07-e054-00144ff8d46c

Use it

Look up 10866-0685 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10866-0685 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10866-0685. 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.