ALCOHOL-FREE ANTICAVITY
- Product NDC
- 71141-482
- 11-digit product format
- 711410482
- Labeler code
- 71141
- Product ID
- 71141-482_5b9c753e-8b93-524b-e063-6294a90a297d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL-FREE ANTICAVITY
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Lidl US, LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-16
- Substance
- SODIUM FLUORIDE
- Active strength
- .1 mg/mL
- 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
- ALCOHOL-FREE ANTICAVITY
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | .1 mg/mL |
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 |
|---|---|---|---|---|---|---|---|
| 71141-482-86 | 71141048286 | 1000 mL in 1 BOTTLE, PLASTIC (71141-482-86) | 1000 ml | 2026-09-16 | No | No | Current |