Home NDC 42961-237-01 NDC 42961-237-01 - Xpect Hydrocortisone 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 42961-237
Requested NDC 42961-237-01
Package NDCs from labels 42961-237-01, 42961-237-02, 42961-237-03, 42961-237-04
Manufacturer Cintas Corporation | SAFETEC OF AMERICA, INC
Effective date 2025-09-26
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 42961-237-01 Xpect Hydrocortisone 0.9 g in 1 PACKET CREAM 0.9 3 42961-237-02 Xpect Hydrocortisone 10 in 1 BOX CREAM 10 3 42961-237-03 Xpect Hydrocortisone 20 in 1 BOX CREAM 20 3 42961-237-04 Xpect Hydrocortisone 10 in 1 BAG CREAM 10 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 42961-237 XPECT HYDROCORTISONE (HYDROCORTISONE) CREAM [CINTAS CORPORATION] 2 Current NDC, 4 package rows 20241228_45ef9be4-54c4-4d85-966b-27708313ded4.zip
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 125 of 338 · 6,756 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 unii: WI4X0X7BPJ 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 Pain Release MENTHOL Natures Formulae Health Products Ltd. 781dfd66-f006-a2d7-e053-2991aa0a170c 2025-12-29 Warnings Exact identifier application number: M017 Pain Release MENTHOL Natures Formulae Health Products Ltd. 781d53cf-b3df-3e2b-e053-2a91aa0a7dcd 2025-12-29 Warnings Exact identifier application number: M017 Trauma Less MENTHOL Natures Formulae Health Products Ltd. 781e94d5-1d34-7202-e053-2991aa0ae768 2025-12-29 Warnings Exact identifier application number: M017 SnugZ Hand Sanitizing Spry HAND SANITIZER SPRAY SnugZ/USA, LLC 9391bc26-57e6-daec-e053-2995a90a1eb6 2025-12-29 Warnings Exact identifier unii: 3K9958V90M SnugZ Beaded Hand Sanitizer Gel BEADED HAND SANITIZER GEL SnugZ/USA, LLC 6deb1142-dfba-a72b-e053-2991aa0aba43 2025-12-29 Warnings Exact identifier unii: 3K9958V90M SnugZ Hand Sanitizing Wipes HAND SANITIZING WIPES SnugZ/USA, LLC c5d9122a-2c67-2387-e053-2a95a90a2c3a 2025-12-29 Warnings Exact identifier unii: 3K9958V90M SnugZ Hand Sanitizer Gel HAND SANITIZER GEL SnugZ/USA, LLC 69bc7a80-0898-4c08-e053-2a91aa0a87a9 2025-12-29 Warnings Exact identifier unii: 3K9958V90M 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 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 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 talc-free medicated body MENTHOL Davion, Inc 27b9b4dc-4d4f-4e9d-b388-a7c6807a0e9b 2025-12-29 Warnings Exact identifier application number: M017 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 Maximum Strength Medicated Foot Powder MENTHOL Davion, Inc 7b442d99-ac19-4f65-828d-954c5350ef5a 2025-12-29 Warnings Exact identifier application number: M017 OCUFRESH WATER Optics Laboratory Inc. b8e477a9-66b9-496b-92fb-3d4bbd7b36b5 2025-12-29 Warnings Exact identifier unii: 059QF0KO0R Dehydrated Alcohol ALCOHOL Ajenat Pharmaceuticals LLC 636d6421-cadf-42b3-a431-ba40c06e36d2 2025-12-29 Warnings, Adverse reactions Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.