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Sodium Fluoride 5000 ppm Dry Mouth

NDC 11527-755, Sodium Fluoride, gel, dentifrice, from Sheffield Pharmaceuticals LLC.

Product NDC
11527-755
Status
Listed
Labeler
Sheffield Pharmaceuticals LLC
Dosage form
GEL, 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/11527-755 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE6.1 mg/mL
Package NDCNDC-11Package
11527-755-34115270755341 TUBE in 1 CARTON (11527-755-34) / 100 mL in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cbc67f03-55c4-4781-ba37-87c737b60282

  • NADAC price for package 11527075534

    GET /v1/drugs/nadac/11527075534

Use it

Look up 11527-755 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/11527-755 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 11527-755. 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.