Seavue Dental Desensitizer
- Product NDC
- 87118-003
- 11-digit product format
- 871180003
- Labeler code
- 87118
- Product ID
- 87118-003_3f47f399-1a15-5264-e063-6394a90aeb1c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- potassium nitrate and sodium fluoride dentifrice
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Xiling (Zhenjiang) Medical Technology Co., Ltd.
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-08
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 26; 1.36 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Seavue Dental Desensitizer
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM NITRATE | 26 mg/g |
| SODIUM FLUORIDE | 1.36 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | RU45X2JN0Z, 8ZYQ1474W7 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87118-003-01 | Seavue Dental Desensitizer | 1 g in 1 BOX | GEL, DENTIFRICE | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87118-003-01 | 87118000301 | 1 g in 1 BOX (87118-003-01) | 1 g | 2025-10-08 | No | No | Current |