NDC 68229-403-01 - Alocane Emergency Burn Pads
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
- 68229-403
- Requested NDC
- 68229-403-01
- Package NDCs from labels
- 68229-403-01, 68229-403-02, 68229-403-03
- Manufacturer
- Quest Products, Inc. | Fill Tech USA
- Effective date
- 2026-10-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Alocane Emergency Burn Pads - Quest Products, Inc. | Fill Tech USA | Quest Products, Inc. | Fill Tech USA | 2026-10-22 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| Effective | Related label |
|---|---|
| 2020-02-03 | Alocane ® Emergency Burn Pads |
| 2020-02-03 | Alocane ® Emergency Burn Pads |
| 2020-01-31 | Alocane ® Emergency Burn Pads |
| 2020-01-31 | Alocane ® Emergency Burn Pads |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68229-403-01 | Alocane Emergency Burn Pads | 3 mL in 1 POUCH | SWAB | 3 | 7 | |
| 68229-403-02 | Alocane Emergency Burn Pads | 10 in 1 BOX | SWAB | 10 | 7 | |
| 68229-403-03 | Alocane Emergency Burn Pads | 12 in 1 BOX | SWAB | 12 | 7 |
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.