Opalescence Whitening Complete
- Product NDC
- 51206-452
- 11-digit product format
- 512060452
- Labeler code
- 51206
- Product ID
- 51206-452_5d697a07-5e16-3855-e063-6294a90a16dd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Opalescence Whitening Complete
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Ultradent Products, Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-25
- Substance
- STANNOUS FLUORIDE
- Active strength
- 1.1 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Opalescence Whitening Complete
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| STANNOUS FLUORIDE | 1.1 mg/g |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 51206-452-01 | 51206045201 | 1 TUBE in 1 CARTON (51206-452-01) / 133 g in 1 TUBE | 1 tube | 2026-06-25 | No | No | Current |
| 51206-452-02 | 51206045202 | 12 CARTON in 1 PACKAGE, COMBINATION (51206-452-02) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE | 12 carton | 2026-06-25 | No | No | Current |