NDC 10819-4077-01 - Prevantics Swabstick
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
- 10819-4077
- Requested NDC
- 10819-4077-01
- Package NDCs from labels
- 10819-4077-1, 10819-4077-4, 10819-4077-2, 10819-4077-3, 10819-4077-01
- Manufacturer
- Professional Disposables International, Inc.
- Effective date
- 2025-02-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Prevantics Swabstick - Professional Disposables International, Inc. | Professional Disposables International, Inc. | 2025-02-10 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10819-4077-1 | Prevantics Swabstick | 1.6 mL in 1 POUCH | SOLUTION | 1.6 | 3 | |
| 10819-4077-2 | Prevantics Swabstick | 500 in 1 CASE | SOLUTION | 500 | 3 | |
| 10819-4077-2 | Prevantics Swabstick | 1.6 mL in 1 POUCH | SOLUTION | 1.6 | 3 | |
| 10819-4077-3 | Prevantics Swabstick | 500 in 1 CASE | SOLUTION | 500 | 3 | |
| 10819-4077-3 | Prevantics Swabstick | 1.6 mL in 1 POUCH | SOLUTION | 1.6 | 3 | |
| 10819-4077-4 | Prevantics Swabstick | 50 in 1 BOX | SOLUTION | 50 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10819-4077 | PREVANTICS SWABSTICK (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL) SOLUTION [PROFESSIONAL DISPOSABLES INTERNATIONAL, INC.] | 3 | Current NDC, Legacy NDC, 6 package rows | 20250212_9841200b-d4c6-b40c-e053-2995a90a5596.zip |
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.