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NDC 66975-782, 1.1% Sodium Fluoride, paste, dentifrice, from Benco Dental.

Product NDC
66975-782
Status
Listed
Labeler
Benco Dental
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/66975-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE.11 g/100g
Package NDCNDC-11Package
66975-782-0166975078201113 g in 1 TUBE (66975-782-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4e6c48c6-bce2-aa33-e063-6394a90a9659

Use it

Look up 66975-782 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/66975-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 66975-782. 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.