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 Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dr. Scholl's Blister Pain Relief Complete Kit | Scholl's Wellness Company LLC | Shanghai Sibei Cosmetic Co., Ltd. | 2024-12-18 | HUMAN OTC DRUG LABEL |
| Dr. Scholl's Blister Pain Relief Complete Kit | Scholl's Wellness Company LLC | Shanghai Sibei Cosmetic Co., Ltd. | 2024-12-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| 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 | 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.
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| pain relief roll-on | LIDOCAINE 4% | Bionpharma Inc. | f607b6dc-8d13-604a-e053-2995a90a59ab | 2024-12-23 | Warnings | M017 |
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| Kids SPF50 Plus Mineral Sunscreen Continuous Totally Tropical | ZINC OXIDE AND TITANIUM DIOXIDE | KAS Direct LLC dba BabyGanics | d5ffe993-de8f-4623-a010-9cb8dd70de07 | 2024-12-23 | Warnings | 15FIX9V2JP |
| CERAVE Hydrating Mineral Sunscreen Light Sheer Tint Broad Spectrum SPF 30 | TITANIUM DIOXIDE AND ZINC OXIDE | LOreal USA Products Inc | 8b298516-70df-47ab-834f-51dcde28a43a | 2024-12-23 | Warnings | 15FIX9V2JP |
| Veneno de Abeja Aceite De Vibora Brand | METHYL SALICYLATE | Miramar Cosmetics, Inc DBA Miramar Lab | a6c4889c-e7a9-44b9-bd9a-70fd6e8c4825 | 2024-12-23 | Warnings | M017 |
| Lancome Paris Renergie Lift Makeup Broad Spectrum SPF 27 Sunscreen | OCTINOXATE AND TITANIUM DIOXIDE | SICOS ET CIE | 6a14ee23-28c9-4704-8af9-d1c4db0d9256 | 2024-12-23 | Warnings | 15FIX9V2JP |
| EcoStick Sunscreen SPF 35 | ZINC OXIDE, TITANIUM DIOXIDE | Stream2Sea, LLC | eba17b7a-5e96-4462-9b71-44c2bc577dce | 2024-12-21 | Warnings | 15FIX9V2JP |
| Planet Protecting Sunscreen 30 | TITANIUM DIOXIDE | Stream2Sea, LLC | 89e44c5f-121e-4fdd-b9e0-023909ea32f5 | 2024-12-21 | Warnings | 15FIX9V2JP |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.