United States · FDA National Drug Code directory
Opalescence 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
- 51206-302_5b14d90f-23ec-372b-e063-6294a90a2066
- Product NDC
- 51206-302
- Form
- GEL, DENTIFRICE
- Composition / generic term
- Sodium Fluoride
- Labeler
- Ultradent Products, Inc
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 19940701 / 20300930
Source-listed ingredients
- SODIUM FLUORIDE — 1.1 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 BOX (51206-302-06) / 133 g in 1 TUBE · 51206-302-06
- 1 TUBE in 1 BOX (51206-302-07) / 28.35 g in 1 TUBE · 51206-302-07
- 3 BOX in 1 PACKAGE, COMBINATION (51206-302-08) / 1 TUBE in 1 BOX / 133 g in 1 TUBE · 51206-302-08
- 12 BOX in 1 PACKAGE, COMBINATION (51206-302-09) / 1 TUBE in 1 BOX / 133 g in 1 TUBE · 51206-302-09
- 24 BOX in 1 PACKAGE, COMBINATION (51206-302-10) / 1 TUBE in 1 BOX / 28.35 g in 1 TUBE · 51206-302-10
- 6 BOX in 1 PACKAGE, COMBINATION (51206-302-11) / 1 TUBE in 1 BOX / 133 g in 1 TUBE · 51206-302-11
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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