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 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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| Neutrogena MINERAL UV TINT FACE MEDIUM DEEP SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Acupac Packaging, Inc | 4ee39bbf-b7d7-8f87-e063-6294a90a2539 | 2026-04-07 | Warnings | 15FIX9V2JP |
| Dermatool Nerve Care | LIDOCAINE HCL, MENTHOL | Papalo Group, LLC | 4ee40c96-9350-4c68-e063-6294a90ac812 | 2026-04-07 | Warnings | M017 |
| Nu Colour Bioadaptive BB plus Foundation - Beige | TITANIUM DIOXIDE | NSE Products, Inc. | f74e83fe-41a0-4998-ae53-30ed5af47592 | 2026-04-07 | Warnings | 15FIX9V2JP |
| Burn Relief | LIDOCAINE | CVS Pharmacy, Inc. | 42b3c341-f422-b2b4-e063-6294a90a47b2 | 2026-04-06 | Warnings | M017 98PI200987 |
| KinetiCream Pain Relieving Topical Analgesic | MENTHOL | Phoenix Bioperformance Products LLC | bb4c9e73-e62d-4b8c-a16c-b90db1a8b2a7 | 2026-04-06 | Warnings | M017 |
| KinetiCream Anti-Inflammatory and Pain Relief | MENTHOL | Phoenix Bioperformance Products LLC | 39a6d26b-b5f4-45d7-a9b5-6edbf42d7500 | 2026-04-06 | Warnings | M017 |
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| Pain-Relieving Patch | CAMPHOR, MENTHOL, METHYL SALICYLATE | CVS Pharmacy | 4ecf4a6e-5c0f-7943-e063-6394a90a81cc | 2026-04-06 | Warnings | M017 |
| RAPID RELIEF | 0.025% CAPSAICIN PAIN PATCH | RAPID AID VIET NAM COMPANY LIMITED | 4edbaa1a-6e44-4865-e063-6394a90a8cc3 | 2026-04-06 | Warnings | M017 |
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| NeroCare Capsaicin Neuropathy Relief Cream | CAPSAICIN | Guangzhou Tata Biotechnology Co., Ltd. | 4e89b7eb-0d84-dc57-e063-6394a90a7dd9 | 2026-04-03 | Warnings | M017 |
| KIDS TOOTHPASTE, FOR CAVITY PROTECTION | KIDS TOOTHPASTE FOR CAVITY PROTECTION | Shulisa (Foshan) Daily ChemicalIndustry Co., Ltd | 4e8fab9e-f05c-5e2f-e063-6294a90aecf9 | 2026-04-03 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.