Home NDC 64032-8125 NDC 64032-8125 - Signature Care Cold and Hot Medicated 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 64032-8125
Manufacturer Safeway
Effective date 2024-12-17
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 77 of 228 · 4,555 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Hydrocortisone HYDROCORTISONE AKRON PHARMA INC fa956b6a-1712-4f7a-9490-11866dcd17c8 2025-12-29 Warnings Exact identifier application number: M017 Frankincense and Myrrh Nerve Combo Pack MENTHOL Wise Consumer Products 471d815c-1c34-e0f8-e063-6294a90aca78 2025-12-29 Warnings Exact identifier application number: M017 Pain Release MENTHOL Natures Formulae Health Products Ltd. 781d3c8d-7b70-e973-e053-2991aa0aaa78 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Pain Release MENTHOL Natures Formulae Health Products Ltd. 781dfd66-f006-a2d7-e053-2991aa0a170c 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Fortify MENTHOL Natures Formulae Health Products Ltd. 781d53cf-b3dc-3e2b-e053-2a91aa0a7dcd 2025-12-29 Warnings Exact identifier unii: L7T10EIP3A Pain Release MENTHOL Natures Formulae Health Products Ltd. 781d53cf-b3df-3e2b-e053-2a91aa0a7dcd 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Trauma Less MENTHOL Natures Formulae Health Products Ltd. 781e94d5-1d34-7202-e053-2991aa0ae768 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Quality Choice Cold Therapy Gel MENTHOL Chain Drug Marketing Association, Inc. f9c659cd-e7fa-ac2d-e053-6294a90a2573 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A PAIN RELIEF PATCHES LIDOCAINE Harris Teeter 5a0501e8-bc06-4e33-8db8-93b21a715141 2025-12-29 Warnings Exact identifier application number: M017 Hot and Cold Medicated Patch MENTHOL Harris Teeter 9debd4ef-c21b-41ae-afd1-58f47c51c99c 2025-12-29 Warnings Exact identifier application number: M017 rxcui: 420222 unii: L7T10EIP3A Maximum OTC Strength Feminine Anti-Itch Creme BENZOCAINE, RESORCINOL Quality Choice (CHAIN DRUG MARKETING ASSOCIATION) 0e9a711c-ddf4-af63-e063-6294a90a0ebe 2025-12-29 Warnings Exact identifier application number: M017 Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Harris Teeter 3f5b4eee-49c4-408c-9af2-e7924c26ac63 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A talc-free medicated body MENTHOL Davion, Inc 27b9b4dc-4d4f-4e9d-b388-a7c6807a0e9b 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Medicated Cornstarch Baby Powder ACTIVE CORN STARCH Davion, Inc. e39032d1-c8cd-4a41-af10-126970b8ad38 2025-12-29 Warnings Exact identifier unii: 24H4NWX5CO H-E-B Medicated Corn Starch Foot Powder MENTHOL Davion, Inc a6675e00-bc6b-4466-a283-4cece5f91970 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Maximum Strength Medicated Foot Powder MENTHOL Davion, Inc 7b442d99-ac19-4f65-828d-954c5350ef5a 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A OCUFRESH WATER Optics Laboratory Inc. b8e477a9-66b9-496b-92fb-3d4bbd7b36b5 2025-12-29 Warnings Exact identifier unii: 059QF0KO0R HEB Medicated Cornstarch Body Powder MENTHOL Davion, Inc df1331fb-48df-4f21-8564-0468078fd12d 2025-12-29 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Honest Med Capsaicin Patch CAPSAICIN Proper Buys LLC 30169d44-b1b2-5c0f-e063-6294a90ae159 2025-12-28 Warnings Exact identifier application number: M017 Honest Med Lidocaine Lavender Roll-on LIDOCAINE HCL Proper Buys LLC 2dcd40a9-3fdd-a71e-e063-6294a90a704f 2025-12-28 Warnings Exact identifier application number: M017
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.