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
- 2024-11-05
- 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 | 2024-11-05 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68229-403-02 | 2020-02-03 | C162847 | 48780-1 | 9d75b9d0-8239-f424-e053-dadaa90a57ce | Alocane ® Emergency Burn Pads |
| 68229-403-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-8239-f424-e053-dadaa90a57ce | 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.
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| Bacteriostatic Water | BACTERIOSTATIC WATER | Fujian Genohope Biotech Ltd. | 54f66b82-c9e5-a2bc-e063-6394a90adbbc | 2026-06-23 | 059QF0KO0R | |
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| Roll Pain Away Lavender | CAPSAICIN | PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA | 547ef2d9-f5c7-9de1-e063-6394a90a218b | 2026-06-17 | Warnings | M017 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.