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Opalescence Sensitivity Relief Whitening

NDC 51206-451, Potassium Nitrate and Sodium Fluoride, gel, dentifrice, from Ultradent Products, Inc..

Product NDC
51206-451
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/51206-451 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM NITRATE50 mg/g
  • SODIUM FLUORIDE1.1 mg/g
Package NDCNDC-11Package
51206-451-01512060451011 TUBE in 1 CARTON (51206-451-01) / 133 g in 1 TUBE
51206-451-025120604510212 CARTON in 1 PACKAGE, COMBINATION (51206-451-02) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
51206-451-03512060451031 TUBE in 1 CARTON (51206-451-03) / 28.35 g in 1 TUBE
51206-451-045120604510424 CARTON in 1 PACKAGE, COMBINATION (51206-451-04) / 1 TUBE in 1 CARTON / 28.35 g in 1 TUBE
51206-451-055120604510548 TUBE in 1 PACKAGE, COMBINATION (51206-451-05) / 28.35 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

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

Use it

Look up 51206-451 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51206-451 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51206-451. 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.