Crest
- Product NDC
- 58933-174
- Requested package NDC
- 58933-174-42
- 11-digit product format
- 589330174
- Labeler code
- 58933
- Product ID
- 58933-174_c46d9c7f-4453-0aed-e053-2995a90a503e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Procter & Gamble Manufacturing M
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-12-18
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 2 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58933-174 | CREST BUBBLEGUM (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING MÉXICO, S. DE R.L. DE C.V.] | 7 | Legacy NDC | 20250110_7d628f5b-f5f7-7c85-e053-2a91aa0a99cc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58933-174-42 | 58933017442 | 119 g in 1 TUBE (58933-174-42) | 119 g | 2018-12-18 | 0000-00-00 | No | No | Current |