COLGATE OPTIC WHITE RELIEF
- Product NDC
- 35000-799
- 11-digit product format
- 350000799
- Labeler code
- 35000
- Product ID
- 35000-799_ba37adc9-1716-4f89-83d0-a39f023ddb60
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Colgate-Palmolive Company
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-09
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.1 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 8ZYQ1474W7 | SODIUM FLUORIDE | 7681-49-4 | SODIUM FLUORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 35000-799-59 | 35000079959 | 1 TUBE in 1 CARTON (35000-799-59) / 107 g in 1 TUBE | 1 tube | 2025-10-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| COLGATE ® OPTIC WHITE ® RELIEF | Colgate-Palmolive Company | Mission Hills, S.A. de C.V. | 2025-10-14 | HUMAN OTC DRUG LABEL | 1 |