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 132 of 304 · 6,066 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Up up LIDOCAINE PAIN RELIEF MAXIMUM STRENGTH PATCHES Target Corporation 44121d40-86e1-0df6-e063-6294a90aedaf 2025-11-20 Warnings Exact identifier application number: M017 rxcui: 1737778 unii: 98PI200987 Up up PAIN RELIEF ADVANCED HYDROGEL PATCHES Target Corporation 44128b70-3172-ee37-e063-6294a90a705f 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC f03090fa-f7e6-f53a-e053-2a95a90aa819 2025-11-20 Warnings Exact identifier application number: M017 HEATING PAIN RELIEF METHYL SALICYLATE, MENTHOL SUNSET NOVELTIES, INC ff073e47-3107-e17e-e053-6294a90a58fa 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC fc8a8f20-97ab-481e-e053-6394a90a3525 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL MENTHOL SUNSET PAIN RELIEF ROLL-ON 3OZ 934d4638-b47b-187d-e053-2995a90ae69d 2025-11-20 Warnings Exact identifier application number: M017 FOOT PAIN RELIEF ROLL-ON LIDOCAINE, MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 43edcea0-ab04-f368-e063-6294a90a817a 2025-11-19 Warnings Exact identifier application number: M017 unii: 98PI200987 Sandra Plasencia Green Tea Daily SPF 50 Moisturizer TITANIUM DIOXIDE Sandra Plasencia Skincare 43ef1f93-0e89-0a35-e063-6394a90afb51 2025-11-19 Warnings Exact identifier unii: 15FIX9V2JP Absolut Skin Corticosoothe Anti-Itch HYDROCORTISONE Absolut Skin Incorporated deb52218-9176-4aaa-a22f-b66dada6690f 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy LIDOCAINE InterMed Laboratories Private Limited 43f3d189-f6b7-02ed-e063-6394a90afd73 2025-11-19 Warnings Exact identifier application number: M017 rxcui: 1737778 unii: 98PI200987 Maximum Strength 4% Lidocaine Patch HealthA2Z LIDOCAINE InterMed Laboratories Private Limited 43f3e288-e828-8130-e063-6394a90a6d44 2025-11-19 Warnings Exact identifier application number: M017 rxcui: 1737778 unii: 98PI200987 Maximum Strength 4% Lidocaine Patch Leader LIDOCAINE InterMed Laboratories Private Limited 42f06914-c8b8-ea9c-e063-6294a90a79e6 2025-11-19 Warnings Exact identifier application number: M017 rxcui: 1737778 unii: 98PI200987 Walgreens Lubricant Eye Drops CARBOXYMETHYLCELLULOSE SODIUM Walgreen Company a39864a3-2407-7b7e-e053-2a95a90ab92f 2025-11-19 Warnings Exact identifier unii: K679OBS311 Walgreens Lubricant Eye Drops CARBOXYMETHYLCELLULOSE SODIUM Walgreen Company a39919d5-84db-05df-e053-2995a90ab1d2 2025-11-19 Warnings Exact identifier unii: K679OBS311 CVS Anti-Itch CAMPHOR, MENTHOL CVS 87715662-c788-9a8d-e053-2a95a90acb53 2025-11-19 Warnings Exact identifier application number: M017 Walgreen Anti Itch CAMPHOR, MENTHOL Walgreens b4f47a8d-d4a6-9233-e053-2a95a90afd90 2025-11-19 Warnings Exact identifier application number: M017 Leader Anti-Itch CAMPHOR, MENTHOL LEADER/Cardinal Helath 110, Inc. 9ca985c6-5017-0558-e053-2995a90a8202 2025-11-19 Warnings Exact identifier application number: M017 CVS Anti-Itch PRAMOXINE HCL CVS 87fc476a-5b12-7383-e053-2995a90a530b 2025-11-19 Warnings Exact identifier application number: M017 Walgreen Anti-Itch PRAMOXINE HCL Walgreens b5f9d1c5-891e-4377-e053-2995a90aa281 2025-11-19 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET PAIN RELIEF 89f5f688-856f-f2df-e053-2995a90a73cf 2025-11-19 Warnings Exact identifier application number: M017
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.