OptiRinse Plus
- Product NDC
- 77982-001
- 11-digit product format
- 779820001
- Labeler code
- 77982
- Product ID
- 77982-001_ba492995-a687-43e9-baff-c5f1c3d7b5c2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Remineralizing Fluoride Rinse
- Dosage form
- LIQUID
- Route
- DENTAL
- Labeler
- Laboratoires MSP Inc
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-11-04
- Marketing end
- 0000-00-00
- Substance
- CETYLPYRIDINIUM CHLORIDE; SODIUM FLUORIDE
- Active strength
- 0 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 77982-001-01 | OptiRinse Plus | 500 mL in 1 BOTTLE | LIQUID | 500 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 77982-001 | OPTIRINSE PLUS (REMINERALIZING FLUORIDE RINSE) LIQUID [LABORATOIRES MSP INC] | 2 | Legacy NDC, 1 package rows | 20201107_003a6c1e-b03a-41c9-8d0a-a2ee762ac7fe.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 |
|---|
| 77982-001-01 | 77982000101 | 500 mL in 1 BOTTLE (77982-001-01) | 500 ml | 2020-11-04 | 0000-00-00 | No | No | Current |