Home NDC 59050-059 NDC 59050-059 - 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 59050-059
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 211 · 4,220 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join 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 Walgreen Anti Itch CAMPHOR, MENTHOL Walgreens b4f47a8d-d4a6-9233-e053-2a95a90afd90 2025-11-19 Warnings Exact identifier application number: M017 Leader Anti-Itch CAMPHOR, MENTHOL LEADER/Cardinal Helath 110, Inc. 9ca985c6-5017-0558-e053-2995a90a8202 2025-11-19 Warnings Exact identifier application number: M017 CVS Anti-Itch PRAMOXINE HCL CVS 87fc476a-5b12-7383-e053-2995a90a530b 2025-11-19 Warnings Exact identifier application number: M017 Walgreen Anti-Itch PRAMOXINE HCL Walgreens b5f9d1c5-891e-4377-e053-2995a90aa281 2025-11-19 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET PAIN RELIEF 89f5f688-856f-f2df-e053-2995a90a73cf 2025-11-19 Warnings Exact identifier application number: M017 Itch Eraser DIPHENHYDRAMINE HCL Tender Corporation d/b/a Adventure Ready Brands 2204e135-6a23-68a2-e063-6394a90ac019 2025-11-18 Warnings Exact identifier application number: M017 Analgesic Balm MENTHOL 10%, METHYL SALICYLATE 15% Geri-Care Pharmaceuticals, Corp c8594e10-661f-6ff3-e053-2995a90ab4fc 2025-11-18 Warnings Exact identifier application number: M017 Mag 5 PT Cooling Formula Recovery Cream MENTHOL RENU LABORATORIES, LLC a45cde67-64ec-643b-e053-2a95a90a10b6 2025-11-18 Warnings Exact identifier application number: M017 Sterile Water WATER Fresenius Kabi USA, LLC fd823bef-c14c-4708-a18a-8aaa8470412f 2025-11-18 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R After Ivy Wipe CAMPHOR Tender Corporation d/b/a Adventure Ready Brands 21d98018-826a-1d0d-e063-6294a90a0a71 2025-11-17 Warnings Exact identifier application number: M017
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.