Crest
- Product NDC
- 37000-171
- 11-digit product format
- 370000171
- Labeler code
- 37000
- Product ID
- 37000-171_498c8df4-d3e1-0540-e063-6294a90ab0a9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-12-18
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.5 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Crest
- Brand name suffix
- Strawberry
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1.5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 891775 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37000-171-42 | CrestStrawberry | 119 g in 1 TUBE | PASTE, DENTIFRICE | 119 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37000-171 | CREST STRAWBERRY (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250309_7d51c67b-7409-e5a7-e053-2a91aa0a81fa.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 |
|---|
| 37000-171-42 | 37000017142 | 119 g in 1 TUBE (37000-171-42) | 119 g | 2018-12-18 | 0000-00-00 | No | No | Current |