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 147 of 304 · 6,066 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Perricone MD Neuropeptide Restorative Neck and Chest Therapy Broad Spectrum SPF 25 TITANIUM DIOXIDE THG Beauty USA LLC 23f4cf41-0eed-2df3-e063-6294a90ad402 2025-10-28 Warnings Exact identifier unii: 15FIX9V2JP GoodSense Pain Relief LIDOCAINE Geiss, Destin & Dunn, Inc 826f8da4-8468-ea0a-e053-2991aa0a66cb 2025-10-28 Warnings Exact identifier application number: M017 rxcui: 1737778 unii: 98PI200987 CALMADOL CAMPHOR, MENTHOL, METHYL SALICYLATE GRANDALL DISTRIBUTING, LLC 31b7f84e-8b66-4d31-8e9c-279d0af2fe64 2025-10-28 Warnings Exact identifier application number: M017 XRay DOL CAMPHOR, MENTHOL, AND METHYL SALICYLATE Genomma Lab USA, Inc. e07fef46-68d9-769c-e053-2a95a90aa065 2025-10-28 Warnings Exact identifier application number: M017 CVS Medicated Heat CAPSICUM EXTRACT CVS Pharmacy 81cd1019-93a6-311b-e053-2991aa0a7997 2025-10-28 Warnings Exact identifier application number: M017 Foster and Thrive LIDOCAINE STRATEGIC SOURCING SERVICES, LLC f950b072-d978-b629-e053-6394a90abfaf 2025-10-28 Warnings Exact identifier application number: M017 rxcui: 1737778 unii: 98PI200987 lidocaine LIDOCAINE PHOENIX RX LLC 3a602aee-09e2-892c-e063-6294a90a558f 2025-10-28 Warnings, Adverse reactions Exact identifier unii: 98PI200987 Bacteriostatic Water WATER Henry Schein, Inc. a833502e-a622-4e81-8c58-cef6ccb6c4c9 2025-10-27 Boxed warning, Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R LACRIFRESH HYDRAPF GLYCERIN, POVIDONE AVIZOR, S.A. 41bbd23e-0ec8-eb18-e063-6294a90a46d1 2025-10-27 Warnings Exact identifier unii: PDC6A3C0OX LACRIFRESH HYDRAMAXPF GLYCERIN, POVIDONE AVIZOR, S.A. 41be1604-89b4-7ec3-e063-6294a90a3331 2025-10-27 Warnings Exact identifier unii: PDC6A3C0OX TIBENA EVERYTHING MULTI CUSHION SPF50 HOMOSALATE, TITANIUM DIOXIDE KONAD CO LTD 421eda8f-62b2-30fb-e063-6394a90a4947 2025-10-27 Warnings Exact identifier unii: 15FIX9V2JP Calamine Plus Pramoxine HCl CALAMINE PLUS SPRAY Premier Brands of America, Inc. d3452573-f91f-f157-e053-2a95a90a1ad8 2025-10-27 Warnings Exact identifier application number: M017 PR MENTHOL Amphp, Inc 6f5b9e08-c445-4fac-e053-2a91aa0aa737 2025-10-27 Warnings Exact identifier application number: M017 Lidocaine BURN RELIEF Foodhold USA b25dc0df-02d0-41ac-b36c-2c04baa77ef2 2025-10-27 Warnings Exact identifier application number: M017 unii: 98PI200987 Menthol MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE FSA Store Inc. fb3548c8-f202-dc50-e053-6394a90a5b30 2025-10-27 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE CONTINUOUS SPRAY Premier Brands of America, Inc. d344f68b-9b62-3029-e053-2995a90a1665 2025-10-27 Warnings Exact identifier application number: M017 Up and Up Dry Eye Relief Lubricant Eye Drops CARBOXYMETHYLCELLULOSE SODIUM Target Corporation 3b1834e6-75cf-5380-e063-6294a90ad1d5 2025-10-25 Warnings Exact identifier unii: K679OBS311 Up and Up Dry Eye Relief Lubricant Eye Drops CARBOXYMETHYLCELLULOSE SODIUM Hanlim 420274c6-7bf0-0920-e063-6294a90a30be 2025-10-25 Warnings Exact identifier unii: K679OBS311 Glycerin GLYCERIN DSC Laboratories Inc. 5e97aa5b-62e2-0664-e053-2a91aa0ac341 2025-10-24 Warnings Exact identifier unii: PDC6A3C0OX Glycerin GLYCERIN H E B 3d03ce42-e671-6d76-e054-00144ff8d46c 2025-10-24 Warnings Exact identifier unii: PDC6A3C0OX
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.