Home NDC 44019-520 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 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.
Matched openFDA labels page 82 of 213 · 4,257 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Toothache and Gum Relief Cushions BENZOCAINE Rite Aid 9970d485-0b78-1438-e053-2995a90ad32c 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 Nighttime 4X Medicated Cream BENZOCAINE Rite Aid 21645ed1-2dc0-223a-e063-6394a90ab021 2025-11-21 Warnings Exact identifier application number: M017 unii: U3RSY48JW5 4x Medicated Gum Cream BENZOCAINE Albertsons b81a308c-9c30-0e3d-e053-2a95a90a15d2 2025-11-21 Warnings Exact identifier application number: M017 unii: U3RSY48JW5 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC b0edd9d9-951f-d3dd-e053-2995a90a8d5a 2025-11-21 Warnings Exact identifier application number: M017 Eyewash Additive Concentrate WATER AND PROPYLENE GLYCOL Haws Corporation dd168403-398c-41ff-b1df-d93e4ff39de3 2025-11-20 Warnings Exact identifier unii: 059QF0KO0R Up up LIDOCAINE PAIN RELIEF MAXIMUM STRENGTH PATCHES Target Corporation 44121d40-86e1-0df6-e063-6294a90aedaf 2025-11-20 Warnings Exact identifier application number: M017 MK Alcohol Prep Pads Large ISOPROPYL ALCOHOL Changzhou Maokang Medical Products Co., Ltd f1ff70d7-d0f2-45db-96e9-883b54c6e441 2025-11-20 Warnings Exact identifier unii: ND2M416302 Up up PAIN RELIEF ADVANCED HYDROGEL PATCHES Target Corporation 44128b70-3172-ee37-e063-6294a90a705f 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC f03090fa-f7e6-f53a-e053-2a95a90aa819 2025-11-20 Warnings Exact identifier application number: M017 HEATING PAIN RELIEF METHYL SALICYLATE, MENTHOL SUNSET NOVELTIES, INC ff073e47-3107-e17e-e053-6294a90a58fa 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC fc8a8f20-97ab-481e-e053-6394a90a3525 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL MENTHOL SUNSET PAIN RELIEF ROLL-ON 3OZ 934d4638-b47b-187d-e053-2995a90ae69d 2025-11-20 Warnings Exact identifier application number: M017 FOOT PAIN RELIEF ROLL-ON LIDOCAINE, MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 43edcea0-ab04-f368-e063-6294a90a817a 2025-11-19 Warnings Exact identifier application number: M017 Absolut Skin Corticosoothe Anti-Itch HYDROCORTISONE Absolut Skin Incorporated deb52218-9176-4aaa-a22f-b66dada6690f 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy LIDOCAINE InterMed Laboratories Private Limited 43f3d189-f6b7-02ed-e063-6394a90afd73 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch HealthA2Z LIDOCAINE InterMed Laboratories Private Limited 43f3e288-e828-8130-e063-6394a90a6d44 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Leader LIDOCAINE InterMed Laboratories Private Limited 42f06914-c8b8-ea9c-e063-6294a90a79e6 2025-11-19 Warnings Exact identifier application number: M017 Dukal Alcohol Prep Pad ISOPROPYL ALCOHOL Dukal LLC 953b0dd6-a667-4146-815e-6845aba0309b 2025-11-19 Warnings Exact identifier unii: ND2M416302 Dukal Sterile Alcohol Swabstick ISOPROPYL ALCOHOL Dukal LLC 8e47e9ad-cea4-76a4-e053-2a95a90ae780 2025-11-19 Warnings Exact identifier unii: ND2M416302 CVS Anti-Itch CAMPHOR, MENTHOL CVS 87715662-c788-9a8d-e053-2a95a90acb53 2025-11-19 Warnings Exact identifier application number: M017
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.