Goby Peppermint
- Product NDC
- 62721-0042
- Requested package NDC
- 62721-0042-9
- 11-digit product format
- 627210042
- Labeler code
- 62721
- Product ID
- 62721-0042_c07de0fe-501b-9525-e053-2a95a90a5795
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Lornamead
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-04-21
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 g/100g
- 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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 62721-0042-9 | 62721004209 | 99 g in 1 TUBE (62721-0042-9) | 99 g | 2021-04-21 | 0000-00-00 | No | No | Current |