COLGATE OPTIC WHITE SENSITIVITY RELIEF
- Product NDC
- 35000-093
- 11-digit product format
- 350000093
- Labeler code
- 35000
- Product ID
- 35000-093_e00560d8-73c6-4939-9ba0-36dcad2a6def
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE, POTASSIUM NITRATE
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Colgate-Palmolive Company
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-18
- Substance
- SODIUM FLUORIDE; POTASSIUM NITRATE
- Active strength
- 1.1; 50 mg/g; 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
- COLGATE OPTIC WHITE SENSITIVITY RELIEF
- Brand name suffix
- SOOTHING MINT
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | 1.1 mg/g |
| POTASSIUM NITRATE | 50 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 |
|---|---|---|---|---|---|---|---|
| 35000-093-59 | 35000009359 | 1 TUBE in 1 CARTON (35000-093-59) / 107 g in 1 TUBE | 1 tube | 2026-09-18 | No | No | Current |