Home NDC 75568-024-01 NDC 75568-024-01 - 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
Requested NDC 75568-024-01
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 229 of 301 · 6,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Meijer Ultra Strength Pain Relieving Topical Analgesic CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE Meijer Distribution, Inc 6319b019-8e17-4de1-b4e0-b402288a97d4 2024-11-15 Warnings Exact identifier application number: M017 Meijer Pain Relieving analgesic CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM Meijer Distribution, Inc 9953be94-5768-448f-83de-f5e53a2972cc 2024-11-15 Warnings Exact identifier application number: M017 careone anti itch HYDROCORTISONE American Sales Company 5f7b1435-ebee-4093-847a-79e8d6641404 2024-11-15 Warnings Exact identifier application number: M017 Luminous Sunscreen SPF 50 ZINC OXIDE, TITANIUM DIOXIDE CLINICAL SKIN LLC 26e2b82c-8d7a-7261-e063-6394a90a7c0d 2024-11-14 Warnings Exact identifier unii: 15FIX9V2JP Tiger Balm METHYL SALICYLATE AND MENTHOL Haw Par Healthcare Ltd. 51293a06-5922-4072-ae14-afaba9c1b58e 2024-11-14 Warnings Exact identifier application number: M017 Neutrogena MINERAL UV TINT FACE LIGHT SPF 30 TITANIUM DIOXIDE, ZINC OXIDE Kenvue Brands LLC e7af4f58-90c8-2987-e053-2995a90a416b 2024-11-13 Warnings Exact identifier unii: 15FIX9V2JP Tylenol Precise Warming Pain Relieving LIDOCAINE Kenvue Brands LLC 0c60b607-ade9-68f2-e063-6394a90a4025 2024-11-13 Warnings Exact identifier application number: M017 unii: 98PI200987 Tylenol Precise Pain Relieving LIDOCAINE Kenvue Brands LLC fc1e0451-8c84-729e-e053-6394a90aaba0 2024-11-13 Warnings Exact identifier application number: M017 unii: 98PI200987 Neutrogena Healthy Skin Liquid Makeup Broad Spectrum SPF 20 - Classic Ivory 10 TITANIUM DIOXIDE Kenvue Brands LLC 143e0a1d-305f-9015-e063-6294a90aa025 2024-11-13 Warnings Exact identifier unii: 15FIX9V2JP Neosporin Plus Pain Relief First Aid Antibiotic/Pain Relieving NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE Kenvue Brands LLC 23222e54-d793-4d79-980e-550e32a95742 2024-11-13 Warnings Exact identifier application number: M017 Lidocaine Anorectal LIDOCAINE Patrin Pharma, Inc 456d41fe-8449-4980-9291-d7a3b65a900d 2024-11-13 Warnings Exact identifier unii: 98PI200987 TopCare Pain Relieving Roll-On Topical Analgesic MENTHOL, UNSPECIFIED FORM Topco Associates LLC 48589893-ca67-471d-88bc-92014295ab9f 2024-11-13 Warnings Exact identifier application number: M017 Neutrogena Ultra Sheer Dry-Touch Sunscreen Broad Spectrum SPF 30 TITANIUM DIOXIDE, ZINC OXIDE Kenvue Brands LLC 18e40353-5c95-4d64-e063-6394a90a017c 2024-11-12 Warnings Exact identifier unii: 15FIX9V2JP Neutrogena Healthy Skin Liquid Makeup SPF 20 - Classic Ivory 10 TITANIUM DIOXIDE Kenvue Brands LLC e0ed4537-8146-45e8-e053-2995a90ac51b 2024-11-12 Warnings Exact identifier unii: 15FIX9V2JP Benadryl Extra Strength Itch Stopping DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE Kenvue Brands LLC a1c1b878-d58f-41ff-b7a8-477f28c52667 2024-11-12 Warnings Exact identifier application number: M017 Real Time Pain Relief Maxx Plus Topical Analgesic MENTHOL Real Time Products Inc. fc509a55-594d-4d44-87db-33286e937581 2024-11-12 Warnings Exact identifier application number: M017 Lidocaine Hydrochloride LIDOCAINE HYDROCHLORIDE Acme United Corporation f1f051ad-7e82-9d1a-e053-2a95a90ac7d3 2024-11-12 Warnings Exact identifier application number: M017 HYDROCORTISONE HYDROCORTISONE ALLIED TRADE LINK LLC 26bc238d-3bda-0c29-e063-6394a90a35fb 2024-11-12 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE Acme United Corporation fabcaa3b-d189-bd29-e053-6294a90ae86b 2024-11-12 Warnings Exact identifier application number: M017 ActivICE MENTHOL Medline Industries, LP 8414aea2-52b5-4221-e053-2a91aa0a622e 2024-11-12 Warnings Exact identifier application number: M017
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.