Alcohol-Free Anticavity
- Product NDC
- 11673-482
- Requested package NDC
- 11673-482-86
- 11-digit product format
- 116730482
- Labeler code
- 11673
- Product ID
- 11673-482_07a3fd78-779d-4a1b-a8e5-d2119592335a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-03-09
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 11673-482 | 11673-482-86 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 11673-482-86 | 11673048286 | 1000 mL in 1 BOTTLE, PLASTIC (11673-482-86) | 1000 ml | 2012-03-09 | 0000-00-00 | No | No | Current |