NDC 61040-007 - First Aid Only First Aid/Burn
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
- 61040-007
- Manufacturer
- Acme United Corporation
- Effective date
- 2023-10-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| First Aid Only First Aid/Burn - Acme United Corporation | Acme United Corporation | 2023-10-09 | 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 |
|---|---|---|---|---|---|---|
| Sore Throat | PHENOL GLYCERIN | CVS PHARMACY, INC | 9683bcfb-2f7e-48a4-aa79-500ee8df099a | 2026-03-02 | Warnings | PDC6A3C0OX |
| Isopropyl alcohol 91 percent | ISOPROPYL ALCOHOL | Sam's West, Inc | a9d6778a-e5ad-4e02-9142-4a932540eda7 | 2026-03-02 | Warnings | M003 |
| Icy Hot Lidocaine No-Mess | LIDOCAINE HYDROCHLORIDE | Chattem, Inc. | 347f9a18-8ab6-47d3-9610-5b4e9ca5d53a | 2026-03-02 | Warnings | V13007Z41A |
| Refresh Optive Mega-3 PF | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 | Allergan, Inc. | 326cb5d6-c784-404f-9a13-6d69262dda6e | 2026-03-01 | Warnings | PDC6A3C0OX |
| Gold Bond Maximum Strength Foot Pain Relief | LIDOCAINE HYDROCHLORIDE | Gold Bond Co LLC | 8e469076-2f5a-4de8-8d13-a38c072b9af8 | 2026-03-01 | Warnings | V13007Z41A |
| HealthWise Pain Relief Lidocaine | LIDOCAINE HYDROCHLORIDE | Veridian Healthcare | 48ecbab9-13e0-d0fa-e063-6294a90a6ff2 | 2026-02-28 | Warnings | V13007Z41A |
| Pain Relieving Gel | LIDOCAINE HYDROCHLORIDE | Chain Drug Marketing Association | b55b7253-2fd2-45cc-b94c-e92395ab0d2b | 2026-02-27 | Warnings, Adverse reactions | V13007Z41A |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | Chain Drug Marketing Association | 31e7063e-0ba1-434f-b404-0ec42df634a3 | 2026-02-27 | Warnings, Adverse reactions | M003 |
| Iodine Tincture | IODINE TINCTURE | The Kroger Co. | c70a718f-d51a-455a-9785-ab41c1b1f8b0 | 2026-02-27 | Warnings, Adverse reactions | M003 |
| Moisturizing Antibacterial | BENZALKONIUM CHLORIDE 0.13% | The Kroger Co. | c13d327a-5bb2-43fa-bc0b-9199e7fd3a38 | 2026-02-27 | Warnings, Adverse reactions | F5UM2KM3W7 |
| MedPride Sterile | BENZALKONIUM CHLORIDE | Shield Line LLC | 02f63d50-e4ff-49b6-9f8c-fddceefe65f3 | 2026-02-27 | Warnings | M003 F5UM2KM3W7 |
| Daily Moisturizing | DIMETHICONE | The Kroger Co. | ea8b186c-82d5-4552-bcce-03e56023ea99 | 2026-02-27 | Warnings, Adverse reactions | 92RU3N3Y1O |
| First Aid Antiseptic | POVIDONE-IODINE | Walmart Inc. | c8fa5ed3-0497-4a23-934b-c72ff02c94ae | 2026-02-27 | Warnings, Adverse reactions | M003 |
| Moisturizing Antibacterial | BENZALKONIUM CHLORIDE | Walmart Inc. | f80ea170-bbb6-47a8-af70-d489af7f3ddc | 2026-02-27 | Warnings, Adverse reactions | F5UM2KM3W7 |
| Moisturizing Antibacterial | BENZALKONIUM CHLORIDE | Walmart Inc. | 0001d1cf-f727-4875-a44f-5a51f7b617a4 | 2026-02-27 | Warnings | F5UM2KM3W7 |
| Moisturizing Antibacterial | BENZALKONIUM CHLORIDE | Walmart Inc. | 0beb635e-9f5a-4d80-ad5d-5b92a47c85dc | 2026-02-27 | Warnings | F5UM2KM3W7 |
| Aloe Vera Gel | LIDOCAINE HCL, MENTHOL | Walmart Inc. | 309dcf5b-7166-976a-e063-6394a90af952 | 2026-02-27 | Warnings, Adverse reactions | V13007Z41A |
| Benzalkonium Chloride | BENZALKONIUM CHLORIDE | Walmart Inc. | 99fba457-0eea-4c0b-987f-6a1690f503fb | 2026-02-27 | Warnings, Adverse reactions | F5UM2KM3W7 |
| FIGS - evolvetogether Hand Sanitizer FIGS 01 Ginger - Cedar Scented | ETHYL ALCOHOL | WE EVOLVETOGETHER INC. | 4bd5a36d-06b4-ba41-e063-6294a90aa121 | 2026-02-27 | Warnings | M003 |
| Rapid Repair Healing Cream | ALLANTOIN, DIMETHICONE | June Jacobs Labs LLC | 186c13be-5e41-b9c9-e063-6294a90ad574 | 2026-02-26 | Warnings | 92RU3N3Y1O |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.