Antiseptic Mouth rinse
- Product NDC
- 41520-210
- 11-digit product format
- 415200210
- Labeler code
- 41520
- Product ID
- 41520-210_ca6269c5-59dd-492d-9df3-e2296b855ceb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Eucalyptol
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- American Sales Company
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-08-02
- Marketing end
- 0000-00-00
- Substance
- EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
- Active strength
- 0 kg/100L; kg/100L; kg/100L; kg/100L
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 41520-210-12 | 2025-02-20 | C162847 | 48780-1 | 9d75b9d0-7939-f424-e053-dadaa90a57ce | 8530bc8a-74d4-42a3-a20c-807d31306c21 |
| 41520-210-13 | 2025-02-20 | C162847 | 48780-1 | 9d75b9d0-7939-f424-e053-dadaa90a57ce | 8530bc8a-74d4-42a3-a20c-807d31306c21 |
| 41520-210-69 | 2025-02-20 | C162847 | 48780-1 | 9d75b9d0-7939-f424-e053-dadaa90a57ce | 8530bc8a-74d4-42a3-a20c-807d31306c21 |
| 41520-210-86 | 2025-02-20 | C162847 | 48780-1 | 9d75b9d0-7939-f424-e053-dadaa90a57ce | 8530bc8a-74d4-42a3-a20c-807d31306c21 |
| 41520-210-12 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-7939-f424-e053-dadaa90a57ce | 8530bc8a-74d4-42a3-a20c-807d31306c21 |
| 41520-210-13 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-7939-f424-e053-dadaa90a57ce | 8530bc8a-74d4-42a3-a20c-807d31306c21 |
| 41520-210-69 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-7939-f424-e053-dadaa90a57ce | 8530bc8a-74d4-42a3-a20c-807d31306c21 |
| 41520-210-86 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-7939-f424-e053-dadaa90a57ce | 8530bc8a-74d4-42a3-a20c-807d31306c21 |