Anitseptic Mouth Rinse
- Product NDC
- 68016-941
- Requested package NDC
- 68016-941-77
- 11-digit product format
- 680160941
- Labeler code
- 68016
- Product ID
- 68016-941_b1e80dce-33d8-4538-a1a3-dbb411b66fad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Eucalyptol, Menthol, Methyl salicylate, Thymol
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Pharmacy Value Alliance LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2003-08-19
- 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
- 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 | 68016-941 | 68016-941-77 | D | Discontinued by firm | 2026-10-15 |
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 |
|---|---|---|---|---|---|---|---|---|
| 68016-941-77 | 68016094177 | 1000 mL in 1 BOTTLE, PLASTIC (68016-941-77) | 1000 ml | 2003-08-19 | 0000-00-00 | No | No | Current |