Mouth Rinse
- Product NDC
- 51143-318
- 11-digit product format
- 511430318
- Labeler code
- 51143
- Product ID
- 51143-318_12fe4e58-941d-4fa3-abe9-88bee3823eea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- EUCALYPTOL, Menthol, Methyl salicylate, Thymol
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Onpoint, Inc
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2009-07-27
- Marketing end
- 0000-00-00
- Substance
- EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
- Active strength
- 1 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 51143-318 | D | Discontinued by firm | 2026-08-03 | ||
| excluded package | package | 51143-318 | 51143-318-12 | D | Discontinued by firm | 2026-08-03 | |
| excluded package | package | 51143-318 | 51143-318-77 | D | Discontinued by firm | 2026-08-03 | |
| excluded package | package | 51143-318 | 51143-318-86 | D | Discontinued by firm | 2026-08-03 |