Crest Pro Health
- Product NDC
- 69423-882
- 11-digit product format
- 694230882
- Labeler code
- 69423
- Product ID
- 69423-882_47e4a650-9481-bc12-e063-6294a90a695d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-01-01
- Substance
- SODIUM FLUORIDE
- Active strength
- .1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Crest Pro Health
- Brand name suffix
- Densify Rinse
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 313029 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69423-882-32 | Crest Pro HealthDensify Rinse | 946 mL in 1 BOTTLE, PLASTIC | RINSE | 946 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69423-882 | CREST PRO HEALTH DENSIFY RINSE (SODIUM FLUORIDE) RINSE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250116_d84fb9f9-f2bc-358a-e053-2995a90abf07.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 |
|---|
| 69423-882-32 | 69423088232 | 946 mL in 1 BOTTLE, PLASTIC (69423-882-32) | 946 ml | 2022-01-01 | 0000-00-00 | No | No | Current |