Auraglow Daily
- Product NDC
- 81740-002
- 11-digit product format
- 817400002
- Labeler code
- 81740
- Product ID
- 81740-002_1a8ffb75-e8f5-4b32-9eee-2f47d0b61182
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Auraglow LLC
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-08-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 2 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81740-002 | AURAGLOW DAILY (SODIUM FLUORIDE) PASTE, DENTIFRICE [AURAGLOW LLC] | 2 | Legacy NDC | 20221108_f9924be1-5467-4abc-8185-47bc11aef59e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81740-002-01 | 81740000201 | 1 TUBE in 1 CARTON (81740-002-01) > 113 g in 1 TUBE | 1 tube | 2021-08-01 | 0000-00-00 | No | No | Current |