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Opalescence Whitening Sensitivity Relief

NDC 51206-315, Potassium Nitrate and Sodium Fluoride, gel, dentifrice, from Ultradent Products, Inc..

Product NDC
51206-315
Status
Listed
Labeler
Ultradent Products, Inc.
Dosage form
GEL, DENTIFRICE
Route
DENTAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M022
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51206-315 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE1.1 mg/g
  • POTASSIUM NITRATE50 mg/g
Package NDCNDC-11Package
51206-315-01512060315011 TUBE in 1 CARTON (51206-315-01) / 133 g in 1 TUBE
51206-315-025120603150212 CARTON in 1 PACKAGE, COMBINATION (51206-315-02) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
51206-315-03512060315031 TUBE in 1 CARTON (51206-315-03) / 28 g in 1 TUBE
51206-315-045120603150424 CARTON in 1 PACKAGE, COMBINATION (51206-315-04) / 1 TUBE in 1 CARTON / 28 g in 1 TUBE
51206-315-055120603150548 CARTON in 1 PACKAGE, COMBINATION (51206-315-05) / 1 TUBE in 1 CARTON / 28 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 51206-315 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51206-315 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51206-315. 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.