Evo Purple Whitening AntiCavity Fluoride Mouthwash
- Product NDC
- 73928-700
- 11-digit product format
- 739280700
- Labeler code
- 73928
- Product ID
- 73928-700_5d613028-ea95-2d55-e063-6394a90a61e9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Kingkey MBC Life Technology Group co., LTD.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-01
- Substance
- SODIUM FLUORIDE
- Active strength
- .05 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Evo Purple Whitening AntiCavity Fluoride Mouthwash
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | .05 g/100mL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 73928-700-01 | 73928070001 | 296 mL in 1 BOTTLE (73928-700-01) | 296 ml | 2026-09-01 | No | No | Current |