NDC 86818-004-01 - Zetox Antibacterial Wet Wipes
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 86818-004
- Requested NDC
- 86818-004-01
- Package NDCs from labels
- 86818-004-01, 86818-004-02, 86818-004-03, 86818-004-04, 86818-004-05, 86818-004-06
- Manufacturer
- SCK ZETA DIS TICARET
- Effective date
- 2022-01-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Zetox Antibacterial Wet Wipes - SCK ZETA DIS TICARET | SCK ZETA DIS TICARET | 2022-01-23 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 86818-004-02 | 2024-01-30 | C162847 | 48780-1 | 1030e365-3d90-111a-e063-dadaa90a10e2 | Zetox Antibacterial Wet Wipes |
| 86818-004-04 | 2024-01-30 | C162847 | 48780-1 | 1030e365-3d90-111a-e063-dadaa90a10e2 | Zetox Antibacterial Wet Wipes |
| 86818-004-06 | 2024-01-30 | C162847 | 48780-1 | 1030e365-3d90-111a-e063-dadaa90a10e2 | Zetox Antibacterial Wet Wipes |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86818-004-01 | Zetox Antibacterial Wet Wipes | 0.74 g in 1 PATCH | CLOTH | 0.74 | 3 | |
| 86818-004-02 | Zetox Antibacterial Wet Wipes | 120 in 1 PACKAGE | CLOTH | 120 | 3 | |
| 86818-004-03 | Zetox Antibacterial Wet Wipes | 0.74 g in 1 PATCH | CLOTH | 0.74 | 3 | |
| 86818-004-04 | Zetox Antibacterial Wet Wipes | 100 in 1 PACKAGE | CLOTH | 100 | 3 | |
| 86818-004-05 | Zetox Antibacterial Wet Wipes | 0.74 g in 1 PATCH | CLOTH | 0.74 | 3 | |
| 86818-004-06 | Zetox Antibacterial Wet Wipes | 80 in 1 PACKAGE | CLOTH | 80 | 3 |
DailyMed Dashboard NDC Coverage#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.