SENSODYNE
- Product NDC
- 0135-0632
- 11-digit product format
- 001350632
- Labeler code
- 0135
- Product ID
- 0135-0632_130996db-a928-a40f-e063-6394a90acf4e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- stannous fluoride
- Dosage form
- PASTE
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-07-08
- Substance
- STANNOUS FLUORIDE
- Active strength
- 1.1 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
- SENSODYNE
- Brand name suffix
- Rapid Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| STANNOUS FLUORIDE | 1.1 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3FTR44B32Q |
| Rxcui | 416784 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0135-0632-01 | SENSODYNERapid Relief | 96.4 g in 1 TUBE | PASTE | 96.4 | | 11 |
| 0135-0632-01 | SENSODYNERapid Relief | 1 in 1 CARTON | PASTE | 1 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0135-0632 | SENSODYNE RAPID RELIEF (STANNOUS FLUORIDE) PASTE [HALEON US HOLDINGS LLC] | 11 | Current NDC, Legacy NDC, 2 package rows | 20240308_f9589e7c-c5ca-4465-8d37-47ad6c69249f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0135-0632-01 | 00135063201 | 1 TUBE in 1 CARTON (0135-0632-01) / 96.4 g in 1 TUBE | 1 tube | 2019-07-08 | 0000-00-00 | No | No | Current |