DawnMist Fluoride
- Product NDC
- 65517-2018
- 11-digit product format
- 655172018
- Labeler code
- 65517
- Product ID
- 65517-2018_75d5f56a-24f8-5805-e053-2a91aa0aeadc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- Dukal Corporation
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-01-30
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65517-2018 | DAWNMIST FLUORIDE (SODIUM FLUORIDE) PASTE [DUKAL LLC] | 4 | Legacy NDC | 20240709_3c0cbe62-3d3a-4040-ac37-7ca3a988b492.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65517-2018-0 | 65517201800 | 17 g in 1 TUBE (65517-2018-0) | 17 g | 2014-01-30 | 0000-00-00 | No | No | Current |