United States · FDA National Drug Code directory

Opalescence Sensitivity Relief Whitening

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
51206-308_5b14ddfe-ec8e-3a25-e063-6294a90afe5b
Product NDC
51206-308
Form
GEL, DENTIFRICE
Composition / generic term
Potassium Nitrate and Sodium Fluoride
Labeler
Ultradent Products, Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20151130 / 20301013

Source-listed ingredients

  • POTASSIUM NITRATE — 50 mg/g
  • SODIUM FLUORIDE — 1.1 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (51206-308-01) / 28.35 g in 1 TUBE · 51206-308-01
  • 1 TUBE in 1 CARTON (51206-308-02) / 133 g in 1 TUBE · 51206-308-02
  • 3 CARTON in 1 PACKAGE, COMBINATION (51206-308-03) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE · 51206-308-03
  • 12 CARTON in 1 PACKAGE, COMBINATION (51206-308-04) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE · 51206-308-04
  • 24 CARTON in 1 PACKAGE, COMBINATION (51206-308-05) / 1 TUBE in 1 CARTON / 28.35 g in 1 TUBE · 51206-308-05
  • 6 CARTON in 1 PACKAGE, COMBINATION (51206-308-06) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE · 51206-308-06

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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