Crest 3D White
- Product NDC
- 69423-838
- 11-digit product format
- 694230838
- Labeler code
- 69423
- Product ID
- 69423-838_47e5179c-5fa4-860c-e063-6294a90a6462
- 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
- 2015-07-20
- 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 3D White
- Brand name suffix
- Brilliance Pro 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, 1658137 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69423-838-32 | Crest 3D WhiteBrilliance Pro Rinse | 946 mL in 1 BOTTLE, PLASTIC | RINSE | 946 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69423-838 | CREST 3D WHITE BRILLIANCE PRO RINSE (SODIUM FLUORIDE) RINSE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] | 3 | Current NDC, 1 package rows | 20250116_13a01190-a6f3-17b3-e063-6294a90a36c2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69423-838-32 | 69423083832 | 946 mL in 1 BOTTLE, PLASTIC (69423-838-32) | 946 ml | 2015-07-20 | No | No | Historical |