evo ON-THE-GO ANTI-CAVITY FLUORIDE-SPEARMINT
- Product NDC
- 70108-246
- Requested package NDC
- 70108-246-01
- 11-digit product format
- 701080246
- Labeler code
- 70108
- Product ID
- 70108-246_c3e3861a-bf79-47fa-b484-9b51ee9b9e54
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Ashtel Studios, Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-20
- 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 ON-THE-GO ANTI-CAVITY FLUORIDE-SPEARMINT
- 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 |
|---|---|---|---|---|---|---|---|
| 70108-246-01 | 70108024601 | 10 PACKET in 1 POUCH (70108-246-01) / 10 mL in 1 PACKET | 10 packet | 2026-10-20 | No | No | Current |