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 122 of 213 · 4,257 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Melt Pain Away CAPSAICIN Proximity Capital Partners LLC dba Asutra a95a11d7-a2ae-6654-e053-2a95a90a802c 2025-06-18 Warnings Exact identifier application number: M017 Recovery Roll-On MENTHOL, CAMPHOR PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA ebc9630f-6d8b-e4f0-e053-2995a90a0b49 2025-06-18 Warnings Exact identifier application number: M017 ProCure Hydrocortisone 1% HYDROCORTISONE Twin Med LLC 37cdfabc-1fdb-246a-e063-6394a90a008a 2025-06-17 Warnings Exact identifier application number: M017 ProCure Hydrocortisone 1% HYDROCORTISONE Twin Med LLC 37ce6c35-b211-43de-e063-6294a90ab773 2025-06-17 Warnings Exact identifier application number: M017 Universal 70% Rubbing Alcohol with Wintergreen and Glycerin ISOPROPYL ALCOHOL Universal Distribution Center LLC 1fdff866-f534-4c16-b755-b2efd1e6e837 2025-06-17 Warnings Exact identifier unii: ND2M416302 WISH RUBBING ALCOHOL 99% WINTERGREEN ISOPROPYL ALCOHOL LJ Pharma de7b2253-7f36-4a27-8838-442ec635f69b 2025-06-16 Warnings Exact identifier unii: ND2M416302 WISH RUBBING ALCOHOL 70% WINTERGREEN ISOPROPYL ALCOHOL LJ Pharma 98ebf7a7-7c13-4feb-90b5-21cc6dab99f6 2025-06-16 Warnings Exact identifier unii: ND2M416302 Hydrocortisone with Aloe HYDROCORTISONE CREAM 1% Sun Pharmaceutical Industries, Inc. 312ddc8d-100e-cfac-e063-6294a90acd09 2025-06-16 Warnings Exact identifier application number: M017 Curist 5% Lidocaine LIDOCAINE 5% Little Pharma, Inc. f20241a2-c5b1-f124-e053-2995a90a891b 2025-06-16 Warnings Exact identifier application number: M017 Toast Screamin Menthol MENTHOL IDEAZ, LLC 37b48b1a-ef3d-afdc-e063-6294a90a6610 2025-06-16 Warnings Exact identifier application number: M017 Toast Freezin Cold MENTHOL, METHYL SALICYLATE IDEAZ, LLC 37b4d363-0099-8cd3-e063-6394a90a18d6 2025-06-16 Warnings Exact identifier application number: M017 Iolite-S BENZOCAINE Dharma Research, Inc. b3b68914-2adc-4f07-9521-0b18756be522 2025-06-14 Warnings Exact identifier unii: U3RSY48JW5 HAND-I-SAN 75% ISOPROPYL ALCOHOL HAND SANITIZER ZECO, LLC 37627a51-cf31-013c-e063-6294a90ae13a 2025-06-13 Warnings Exact identifier unii: ND2M416302 Earths Care Anti-Itch CAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORM DLC Laboratories, Inc. ba65f58a-d590-498a-b8e7-a3d78935d880 2025-06-13 Warnings Exact identifier application number: M017 Lidocaine LIDOCAINE Stratus Pharmaceuticals Inc 5eb6574c-2066-4390-befc-8e5d2dd6ede2 2025-06-12 Warnings Exact identifier application number: M017 CHINESE RED TIGER LIDOCAINE PATCHES 4% LIDOCAINE, 1%MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 36b9a7a2-5832-4ce5-e063-6294a90aed12 2025-06-12 Warnings Exact identifier application number: M017 PRO COLD HOT Pain Relief Gel Roll-On (Plantar Fasciitis) MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 375bc794-3289-e610-e063-6294a90a4f9b 2025-06-12 Warnings Exact identifier application number: M017 Methyl Salicylate 10% Pain Relieving METHYL SALICYLATE PureTek Corporation 376493eb-5142-db6d-e063-6294a90a1e73 2025-06-12 Warnings Exact identifier application number: M017 Free and Pure Cold Therapy Pain Relief MENTHOL Walgreen Co. 22cbbffc-f876-411e-e063-6394a90a1b38 2025-06-12 Warnings Exact identifier application number: M017 Methylten 25% Pain Relieving METHYL SALICYLATE PureTek Corporation 3767b97e-ab0c-ac26-e063-6394a90a00cf 2025-06-12 Warnings Exact identifier application number: M017
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.