Home NDC 61040-229 NDC 61040-229 - Hydrocortisone 1% Anti-ItchCream 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 61040-229
Manufacturer Acme United Corporation | Acme United Crporation
Effective date 2026-06-13
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 117 of 176 · 3,520 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join HERSTAT PLUS Cold Sore Treatment CAMPHOR, MENTHOL Herstat (USA) Inc. e20ea714-663d-c4ac-e053-2a95a90a5ecc 2025-01-18 Warnings Exact identifier application number: M017 HYDROCORTISONE HYDROCORTISONE DIRECT RX c28c3ceb-1807-b43b-e053-2995a90a2aba 2025-01-17 Adverse reactions Exact identifier rxcui: 106258 unii: WI4X0X7BPJ VITAMIN A and D WHITE PETROLATUM VIVE HEALTH LLC 2bd4465b-6e46-51e2-e063-6294a90a695f 2025-01-16 Warnings Exact identifier unii: B6E5W8RQJ4 VITAMIN A and D WHITE PETROLATUM VIVE HEALTH LLC 2bd4a2b0-f586-3ab1-e063-6294a90aa1ed 2025-01-16 Warnings Exact identifier unii: B6E5W8RQJ4 Pain Relief Medicated CAMPHOR MENTHOL METHYL SALICYTATE RITE AID CORPORATION 60895211-69f3-478b-a33f-1c2071f62950 2025-01-16 Warnings Exact identifier application number: M017 Elgin Pain Relief MENTHOL Eco-Logics, Inc. 70eda21e-e566-42f4-9a49-b0d3ad000652 2025-01-16 Warnings Exact identifier application number: M017 Curist Lidocaine Patch Maximum Strength LIDOCAINE Little Pharma, Inc. e574c188-cc65-287d-e053-2995a90a5972 2025-01-16 Warnings Exact identifier application number: M017 Equate Hydrocortisone Topical HYDROCORTISONE WalMart 1f64555d-f77e-4a83-b222-fdb3ed7d8853 2025-01-16 Warnings Exact identifier application number: M017 rxcui: 106258 unii: WI4X0X7BPJ Equate Hydrocortisone HYDROCORTISONE WalMart f5c32b4a-1159-4b7a-b8ac-256d53020dc2 2025-01-16 Warnings Exact identifier application number: M017 rxcui: 106258 unii: WI4X0X7BPJ Lidocaine Pain Relief Gel-Patch LIDOCAINE Guangzhou Zhupuyou E-commerce Co., Ltd 296fcc36-563f-19ca-e063-6394a90ab3ae 2025-01-15 Warnings Exact identifier application number: M017 K19 RELIEF MENTHOL K19 LLC e2e1ca96-1ae8-4c99-b8de-ce26754292f9 2025-01-15 Warnings Exact identifier application number: M017 Anecream LIDOCAINE 4% Focus Health Group 2d7706e2-7363-4047-96cb-85b718277e8c 2025-01-15 Warnings Exact identifier application number: M017 Boroleum CAMPHOR, MENTHOL, WHITE PETROLATUM Reliable 1 Laboratories 846568af-0fdd-a80e-e053-2a91aa0a9c9e 2025-01-15 Warnings Exact identifier application number: M017 unii: B6E5W8RQJ4 LidoPro Pain Relief CAPSAICIN AND LIDOCAINE Advanced Rx of Tennessee, LLC 27d5997b-1cc2-41c2-e063-6394a90ac74a 2025-01-15 Warnings Exact identifier application number: M017 Pain Relief Patch 4% Lidocaine LIDOCAINE Reliable 1 Laboratories LLC 2b624763-c310-63d9-e063-6394a90a1928 2025-01-15 Warnings Exact identifier application number: M017 Cannarelief 1000mg MENTHOL Carolina Cannabis Creations LLC 01e2ae1a-c969-6dd2-e063-6394a90a9d9e 2025-01-15 Warnings Exact identifier application number: M017 Healing Hand Cream 2000mg MENTHOL Carolina Cannabis Creations LLC 01f8795b-9f95-c793-e063-6394a90a8330 2025-01-15 Warnings Exact identifier application number: M017 CBD Clinic Deep-Rub Pain Relief - Level 5 CAMPHOR, MENTHOL ABACUS HEALTH PRODUCTS, INC. 31e2e5cd-d33e-f058-e063-6394a90af7d2 2025-01-14 Warnings Exact identifier application number: M017 Meijer Odor Free Analgesic Pain Relieving Topical Analgesic LIDOCAINE HYDROCHLORIDE Meijer Distribution, Inc 6288efea-f636-4eea-bb9f-78aa2f9af54a 2025-01-14 Warnings Exact identifier application number: M017 IKONIK TONIK LIDOCAINE HYDROCHLORIDE IKONIK CARE, LLC 122fdfe8-b5fa-46d1-9fd9-3df9887ed320 2025-01-14 Warnings Exact identifier application number: M017
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.