Orbitol
- Product NDC
- 69939-309
- 11-digit product format
- 699390309
- Labeler code
- 69939
- Product ID
- 69939-309_90b48ad5-b8e7-5ee7-e053-2995a90a8097
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM MONOFLUOROPHOSPHATE
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- COSMOPHARM LTD.
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-06-30
- Marketing end
- 2022-06-16
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69939-309-02 | 69939030902 | 145 g in 1 TUBE (69939-309-02) | 145 g | 2016-06-30 | 2022-06-16 | No | No | Current |