Supersmile
- Product NDC
- 53567-0769
- Requested package NDC
- 53567-0769-1
- 11-digit product format
- 535670769
- Labeler code
- 53567
- Product ID
- 53567-0769_d1f064a8-2b95-a7b7-e053-2a95a90ac653
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Monofluorophosphate
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL; ORAL
- Labeler
- Robell Research, Inc.
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-11-23
- Marketing end
- 0000-00-00
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- 1 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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 53567-0769-1 | 53567076901 | 227 g in 1 TUBE (53567-0769-1) | 227 g | 2021-11-23 | 0000-00-00 | No | No | Current |