Opalescence Whitening Sensitivity Relief
- Product NDC
- 51206-315
- 11-digit product format
- 512060315
- Labeler code
- 51206
- Product ID
- 51206-315_5b14ca86-96a0-7c20-e063-6394a90af5bd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Potassium Nitrate and Sodium Fluoride
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Ultradent Products, Inc.
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-08
- Marketing end
- 2030-12-31
- Substance
- SODIUM FLUORIDE; POTASSIUM NITRATE
- Active strength
- 1.1; 50 mg/g; mg/g
- NDC exclude flag
- No
- 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 Sensitivity Relief
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | 1.1 mg/g |
| POTASSIUM NITRATE | 50 mg/g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 8ZYQ1474W7 | Internal UNII lookup |
| RU45X2JN0Z | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1038929 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 44e94663-895b-67da-e063-6394a90a5fe6 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51206-315-01 | Opalescence Whitening Sensitivity Relief | 1 in 1 CARTON | GEL, DENTIFRICE | 1 | 2 | |
| 51206-315-01 | Opalescence Whitening Sensitivity Relief | 133 g in 1 TUBE | GEL, DENTIFRICE | 133 | 2 | |
| 51206-315-02 | Opalescence Whitening Sensitivity Relief | 1 in 1 CARTON | GEL, DENTIFRICE | 1 | 2 | |
| 51206-315-02 | Opalescence Whitening Sensitivity Relief | 12 in 1 PACKAGE, COMBINATION | GEL, DENTIFRICE | 12 | 2 | |
| 51206-315-03 | Opalescence Whitening Sensitivity Relief | 28 g in 1 TUBE | GEL, DENTIFRICE | 28 | 2 | |
| 51206-315-03 | Opalescence Whitening Sensitivity Relief | 1 in 1 CARTON | GEL, DENTIFRICE | 1 | 2 | |
| 51206-315-04 | Opalescence Whitening Sensitivity Relief | 1 in 1 CARTON | GEL, DENTIFRICE | 1 | 2 | |
| 51206-315-04 | Opalescence Whitening Sensitivity Relief | 24 in 1 PACKAGE, COMBINATION | GEL, DENTIFRICE | 24 | 2 | |
| 51206-315-05 | Opalescence Whitening Sensitivity Relief | 1 in 1 CARTON | GEL, DENTIFRICE | 1 | 2 | |
| 51206-315-05 | Opalescence Whitening Sensitivity Relief | 48 in 1 PACKAGE, COMBINATION | GEL, DENTIFRICE | 48 | 2 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Iolite | BENZOCAINE | Dharma Research, Inc. | e4b2d22b-00b3-45a6-9b7d-8ee719587059 | 2023-10-09 | Warnings | M022 |
| Iolite | BENZOCAINE | Dharma Research, Inc. | a0e284f6-292f-4231-8596-f7cee4e0a12f | 2023-10-09 | Warnings | M022 |
| HurriCaine Topical Anesthetic | BENZOCAINE | Beutlich Pharmaceuticals, LLC | fe92637a-c88a-f9dd-e053-6294a90a7fa3 | 2023-07-01 | Warnings | M022 |
| HurriCaine Topical Anesthetic | BENZOCAINE | Beutlich Pharmaceuticals, LLC | c979e958-2042-471a-bf03-e84e68620106 | 2023-06-20 | Warnings | M022 |
| Orajel Gum Pain 3X Medicated | BENZOCAINE, MENTHOL, ZINC CHLORIDE | Church & Dwight Co., Inc. | 9a1632ad-2b47-5653-e053-2995a90ae0d9 | 2023-01-20 | Warnings | M022 |
| KOLORZ TOPICAL ANESTHETIC TRIPLE MINT | BENZOCAINE | DMG AMERICA, LLC | 0f90b227-f938-4e1a-a79e-1967b1a0477e | 2021-10-01 | Warnings | M022 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1038929 | potassium nitrate 5 % / sodium fluoride 0.24 % Toothpaste | PSN | 44e94663-895b-67da-e063-6394a90a5fe6 | 2 |
| 1038929 | potassium nitrate 0.05 MG/MG / sodium fluoride 0.0024 MG/MG Toothpaste | SCD | 44e94663-895b-67da-e063-6394a90a5fe6 | 2 |
| 1038929 | K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste | SY | 44e94663-895b-67da-e063-6394a90a5fe6 | 2 |
| 1038929 | Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste | SY | 44e94663-895b-67da-e063-6394a90a5fe6 | 2 |
| 1038929 | potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste | SY | 44e94663-895b-67da-e063-6394a90a5fe6 | 2 |
| 1038929 | potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.15 % ) Toothpaste | SY | 44e94663-895b-67da-e063-6394a90a5fe6 | 2 |
| 1038929 | potassium nitrate 5 % / sodium fluoride 0.24 % Toothpaste | SY | 44e94663-895b-67da-e063-6394a90a5fe6 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 51206-315-01 | 51206031501 | 1 TUBE in 1 CARTON (51206-315-01) / 133 g in 1 TUBE | 1 tube | 2025-10-08 | 2030-12-31 | No | No | Historical |
| 51206-315-02 | 51206031502 | 12 CARTON in 1 PACKAGE, COMBINATION (51206-315-02) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE | 12 carton | 2025-10-08 | 2030-12-31 | No | No | Historical |
| 51206-315-03 | 51206031503 | 1 TUBE in 1 CARTON (51206-315-03) / 28 g in 1 TUBE | 1 tube | 2025-10-08 | 2030-12-31 | No | No | Historical |
| 51206-315-04 | 51206031504 | 24 CARTON in 1 PACKAGE, COMBINATION (51206-315-04) / 1 TUBE in 1 CARTON / 28 g in 1 TUBE | 24 carton | 2025-10-08 | 2030-12-31 | No | No | Historical |
| 51206-315-05 | 51206031505 | 48 CARTON in 1 PACKAGE, COMBINATION (51206-315-05) / 1 TUBE in 1 CARTON / 28 g in 1 TUBE | 48 carton | 2025-10-08 | 2030-12-31 | No | No | Historical |