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Denta 5000 Plus Sensitive

NDC 16571-823, Sodium fluoride and Potassium nitrate, gel, dentifrice, from Rising Pharma Holdings, Inc..

Product NDC
16571-823
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
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/16571-823 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5.8 mg/mL
  • POTASSIUM NITRATE57.5 mg/mL
Package NDCNDC-11Package
16571-823-1016571082310100 mL in 1 TUBE (16571-823-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/585fb1f5-8c08-43bd-8be4-64adc065d9a2

  • NADAC price for package 16571082310

    GET /v1/drugs/nadac/16571082310

Use it

Look up 16571-823 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16571-823 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16571-823. 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.