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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| Alocane Plus | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | b3ec09b9-7511-0895-e053-2a95a90a7840 | 2025-12-04 | Warnings | M017 V13007Z41A |
| Gold Bond Medicated Pain and Itch Relief | LIDOCAINE HYDROCHLORIDE | Gold Bond Co LLC | d240e9b8-3506-42ab-8a50-05e8d3fac4ff | 2025-12-04 | Warnings | M017 V13007Z41A |
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| AleveX | CAMPHOR AND MENTHOL | Bayer HealthCare LLC | bc66bc1b-c0d5-2481-e053-2a95a90a75de | 2025-12-04 | Warnings | M017 |
| AleveX | CAMPHOR AND MENTHOL | Bayer HealthCare LLC | bafd199a-e198-d5d1-e053-2995a90ad1cb | 2025-12-04 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.