Goby Peppermint
- Product NDC
- 81788-001
- 11-digit product format
- 817880001
- Labeler code
- 81788
- Product ID
- 81788-001_c0539abe-fa93-d4a6-e053-2a95a90a1975
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- BGLG, Inc.
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-05-01
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81788-001-00 | Goby Peppermint | 99 g in 1 TUBE | PASTE | 99 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81788-001 | GOBY PEPPERMINT (SODIUM FLUORIDE) PASTE [BGLG, INC.] | 1 | Legacy NDC, 1 package rows | 20210501_c0541f32-f039-3630-e053-2a95a90a12d6.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 |
|---|
| 81788-001-00 | 81788000100 | 99 g in 1 TUBE (81788-001-00) | 99 g | 2021-05-01 | 0000-00-00 | No | No | Current |