Home NDC 75568-024 NDC 75568-024 - Dr. Scholls Blister Pain Relief Complete 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 75568-024
Package NDCs from labels 75568-024-01
Manufacturer Scholl's Wellness Company LLC | Shanghai Sibei Cosmetic Co., Ltd.
Effective date 2024-12-18
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 75568-024-01 Dr. Scholls Blister Pain Relief Complete 0.37 g in 1 PATCH PATCH 2.96 g 40 mg in 1g 2 75568-024-01 Dr. Scholls Blister Pain Relief Complete 0.37 g in 1 PATCH PATCH 4.44 g 40 mg in 1g 2 75568-024-01 Dr. Scholls Blister Pain Relief Complete 1 in 1 POUCH PATCH 40 mg in 1g 2 75568-024-01 Dr. Scholls Blister Pain Relief Complete 1 in 1 POUCH PATCH 40 mg in 1g 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75568-024 DR. SCHOLLS BLISTER PAIN RELIEF COMPLETE (LIDOCAINE) KIT [SCHOLL'S WELLNESS COMPANY LLC] 2 Unmatched 20250216_26e3a678-b28f-588b-e063-6394a90ac025.zip 75568-024 DR. SCHOLLS BLISTER PAIN RELIEF COMPLETE (LIDOCAINE) KIT [SCHOLL'S WELLNESS COMPANY LLC] 2 Unmatched 20250216_d860b339-48a0-405c-a67d-f7e7a31f6351.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 52 of 307 · 6,130 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Lubricant Eye Drops CARBOXYMETHYLCELLULOSE SODIUM KC Pharmaceuticals, Inc. 4d1d9b3a-ac5f-db27-e063-6294a90afc3f 2026-03-16 Warnings Exact identifier unii: K679OBS311 Lubricant Eye Drops CARBOXYMETHYLCELLULOSE SODIUM Redicare LLC 4d1e5089-22b0-7b3f-e063-6294a90a346a 2026-03-16 Warnings Exact identifier unii: K679OBS311 Shoe Pain Relief LIDOCAINE HCI 4% Sole Amie 0f2ccd5f-b9f4-40fc-b82f-173b0f19bf40 2026-03-16 Warnings Exact identifier application number: M017 LIDOCAINE LIDOCAINE DIRECT RX b8663046-67a4-4858-e053-2a95a90a8aed 2026-03-16 Warnings, Adverse reactions Exact identifier unii: 98PI200987 Lidothol Patch LIDOTHOL PATCH Direct_Rx 1987e839-6f4e-8671-e063-6394a90abea6 2026-03-16 Warnings, Adverse reactions Exact identifier unii: 98PI200987 CVS Muscle Balm MENTHOL, CAMPHOR CVS Health 42796fc4-03be-3b02-e063-6394a90af2ab 2026-03-16 Warnings Exact identifier application number: M017 Crane Safety Hydrocortisone HYDROCORTISONE Crane Safety LLC 96d9527d-9bf7-ce82-e053-2995a90aff0c 2026-03-16 Warnings Exact identifier application number: M017 CVS Health Pain Relief Foot MENTHOL, UNSPECIFIED FORM NATURAL ESSENTIALS, INC. 0f646876-69d0-49db-ade2-2b3eb26dd399 2026-03-16 Warnings Exact identifier application number: M017 Walgreens Cold Therapy Pain Relief Foot Cream MENTHOL Walgreen Co. 3bc8ece3-d555-3efb-e063-6394a90a1981 2026-03-16 Warnings Exact identifier application number: M017 RICHTOFIT RAPID ACTIVE LEG AND FOOT MENTHOL RICHTOFIT LIMITED LIABILITY COMPANY 4c357696-ca96-e6ad-e063-6294a90aaadb 2026-03-16 Warnings Exact identifier application number: M017 HYDRATING TINTED MOISTURIZER SPF50 HYDRATING TINTED MOISTURIZER SPF50 NING PTE. LTD. 4cf8d3d3-eebf-2da0-e063-6294a90a7065 2026-03-14 Warnings Exact identifier unii: 15FIX9V2JP Lidocaine LIDOCAINE Asclemed USA, Inc. e0bfe16f-7a3f-48e0-a2e6-2ec68159a888 2026-03-14 Warnings, Adverse reactions Exact identifier unii: 98PI200987 Xpect Stopain Clinical MENTHOL Cintas Corporation 348e6062-b31e-435e-a153-6aa868b50efa 2026-03-13 Warnings Exact identifier application number: M017 DGH GREASELESS MUSCLE RUB ANALGESIC MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE DOLLAR GENERAL 225abfe0-ec72-4667-96b2-7657e989672b 2026-03-13 Warnings Exact identifier application number: M017 CVS Professional Pain Relief MENTHOL CVS Pharmacy 48836a5b-0baa-b7ee-e063-6294a90ac12b 2026-03-13 Warnings Exact identifier application number: M017 TINTED WATERY SUNSCREEN TITANIUM DIOXIDE, ZINC OXIDE KSISTERS PTE. LTD. 4ced53d0-8bfc-ff8e-e063-6294a90a9dbd 2026-03-13 Warnings Exact identifier unii: 15FIX9V2JP Daily Moisturizing Mineral Sunscreen BROAD SPECTRUM SPF30 EDINA PLASTIC SURGERY,LTD. 4d056e2b-5813-da42-e063-6294a90ac519 2026-03-13 Warnings Exact identifier unii: 15FIX9V2JP Keeps Climax Delay LIDOCAINE HYDROCHLORIDE Cosco International, Inc. 3bfd3173-2dac-40a9-aec3-982b1d47d8fa 2026-03-12 Warnings Exact identifier application number: M017 NanoX Pain Relieving MENTHOL, METHYL SALICYLATE MG Science Technologies LLC 4cc38927-8a8c-2df3-e063-6294a90aa0c1 2026-03-12 Warnings Exact identifier application number: M017 Leader Ultra Lubricating Eye Drops POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL Cardinal Health d7f011a2-05ba-47c3-9519-d31602e105c7 2026-03-12 Warnings Exact identifier unii: 6DC9Q167V3
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.