NDC 44019-520 - First Aid Only Sting Relief Pad
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
- 44019-520
- Manufacturer
- Acme United Corporation
- Effective date
- 2024-11-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| First Aid Only Sting Relief Pad - Acme United Corporation | Acme United Corporation | 2024-11-19 | HUMAN OTC DRUG LABEL |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Chloraspetic | MENTHOL AND BENZOCAINE | Prestige Brands Holdings, Inc. | 2b1808b2-2574-4ab8-a762-5733251848ce | 2024-10-25 | Warnings | U3RSY48JW5 |
| Monistat Care Instant Itch Relief | BENZOCAINE | Insight Pharmaceuticals LLC | 4e9dc791-419f-4c79-aed4-760f8c17a5dd | 2024-10-25 | Warnings | M017 U3RSY48JW5 |
| ZYLOTROL PAIN RELIEVING | LIDOCAINE HCL, MENTHOL | Asclemed USA, Inc. | 1553351c-aee8-4c40-9548-35cce246bda9 | 2024-10-25 | Warnings | M017 |
| Outgro | BENZOCAINE | Medtech Products Inc. | d6be8a1d-aca7-42b1-86da-881d42ffe8d5 | 2024-10-25 | Warnings | M017 U3RSY48JW5 |
| Monistat Complete Care Instant Itch Relief | HYDROCORTISONE | Insight Pharmaceuticals LLC | a0f40504-6183-4f32-8d17-6586b3f386a6 | 2024-10-25 | Warnings | M017 |
| CHLORASEPTIC | MENTHOL AND BENZOCAINE | Prestige Brands Holdings, Inc. | d500f423-b9f2-4d98-8f2a-8bab7c05737c | 2024-10-25 | Warnings | U3RSY48JW5 |
| Boil Ease | BENZOCAINE | Insight Pharmaceuticals LLC | bf108934-5e1a-4059-9dcf-008f52a83fab | 2024-10-25 | Warnings | M017 U3RSY48JW5 |
| CHLORASEPTIC | MENTHOL AND BENZOCAINE | Prestige Brands Holdings, Inc. | b30e4b32-89dd-4e53-81d5-1415105361d4 | 2024-10-25 | Warnings | U3RSY48JW5 |
| Dermarest Eczema Medicated | HYDROCORTISONE | Insight Pharmaceuticals LLC | 0292ab62-5088-45fa-a056-70c2fcc19ef7 | 2024-10-25 | Warnings | M017 |
| anti itch | HYDROCORTISONE | Meijer, Inc. | 2db7bcab-acb8-48ad-8cd1-842ff7765ed9 | 2024-10-23 | Warnings | M017 |
| NATUREANCE MIRACLE | MENTHOL | EROS GLOBAL CORP | ec1a2a1f-a38d-9c59-e053-2a95a90ad268 | 2024-10-23 | Warnings | M017 |
| Profoot Plantar Relief Strips | CAMPHOR (NATURAL), MENTHOL, METHYL SALICYLATE | Rooftop Consumer Health, Inc. | 65e142d8-da21-4c55-9faf-b387cb6c2c0e | 2024-10-23 | Warnings | M017 |
| Profoot Pain Relief Patches | CAMPHOR, MENTHOL, METHYL SALICYLATE | Rooftop Consumer Health, Inc. | cc011b79-2761-40f7-8142-88f8e30a179a | 2024-10-23 | Warnings | M017 |
| Profoot Pain Relief Patches | CAMPHOR, MENTHOL, METHYL SALICYLATE | Profoot, Inc. | 06f82bde-41a1-35f6-e063-6394a90a6437 | 2024-10-23 | Warnings | M017 |
| Isopropyl Rubbing Alcohol 99% | ISOPROPYL ALCOHOL | Universal Distribution Center LLC | 678a9b14-2838-4358-9673-fc23e0f58efb | 2024-10-21 | Warnings | ND2M416302 |
| Deep Cover Bug Bite Relief | BENZOCAINE | Morrisons Outdoors, LLC | 25010dd6-fb48-8ee7-e063-6394a90aee6c | 2024-10-21 | Warnings | M017 U3RSY48JW5 |
| Evel Knievels Natural Choice Pain Relief | MENTHOL, UNSPECIFIED FORM | Natural Essentials, Inc. | 4576656c-4b6e-6965-7665-6c52756c6573 | 2024-10-21 | Warnings | M017 |
| Isopropyl Rubbing Alcohol 70% | ISOPROPYL ALCOHOL | Universal Distribution Center LLC | a9960d2f-f13a-4168-b2e9-d6f4a35d84ae | 2024-10-21 | Warnings | ND2M416302 |
| Isopropyl Rubbing Alcohol 50% | ISOPROPYL ALCOHOL | Universal Distribution Center LLC | 5db1659e-3a13-47f0-90ae-f8f192c6111a | 2024-10-21 | Warnings | ND2M416302 |
| Isopropyl Rubbing Alcohol 70% with Wintergreen | ISOPROPYL ALCOHOL | Universal Distribution Center LLC | 3dcdc1cc-ece8-4b47-a236-ee57c375bb99 | 2024-10-21 | Warnings | ND2M416302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.