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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lidocaine | LIDOCAINE | Cardinal Health 107, LLC | eb808fdf-0420-45e9-ad17-8380d49d5c21 | 2025-10-20 | Warnings, Adverse reactions | 98PI200987 |
| Mountain Ice Sports Recovery | MENTHOL | Mountainside Medical Equipment, Inc. | 98638529-3c17-436e-901f-c8aea52bdab6 | 2025-10-20 | Warnings | M017 |
| Lip Clear Lysine Plus | MENTHOL, UNSPECIFIED FORM | Quantum, Inc. | 21a5b4fb-baed-4766-9820-5c6051c14720 | 2025-10-20 | Warnings | M017 |
| Buzz Away Sting Soothe | MENTHOL | Quantum, Inc. | 419e34ea-17b2-ec32-e063-6394a90a603d | 2025-10-20 | Warnings | M017 |
| Family Care Anti-Itch | HYDROCORTISONE | United Exchange Corp. | deb09e89-9794-89a7-e053-2a95a90abdf8 | 2025-10-20 | Warnings | M017 |
| Numbing Cream | MENTHOL | FlexiGo Inc | 41571c8f-332b-f423-e063-6394a90a8897 | 2025-10-20 | Warnings | M017 |
| Soothing Nerve Therapy | MENTHOL | Wise Consumer Products | 40829d6b-5005-7ec9-e063-6294a90a970e | 2025-10-20 | Warnings | M017 |
| Numbing Cream | MENTHOL | FlexiGo Inc | 4146fd51-b18c-393d-e063-6294a90a4d9a | 2025-10-20 | Warnings | M017 |
| Lidocaine 4% Maximum OTC Strength | LIDOCAINE | Cardinal Health 107, LLC | 975031df-d46d-4098-b1c0-1c0c92b41995 | 2025-10-20 | Warnings | M017 1737778 98PI200987 |
| Cortizone 10 Intensive Healing | HYDROCORTISONE | Chattem, Inc. | bb3d1a3e-4c0c-4694-9c05-80152dd9bd1c | 2025-10-20 | Warnings | M017 |
| Sting relief pad | BENZOCAINE, ALCOHOL | Guangdong Comfort Medical Products Co., Ltd. | 6e905065-10a9-1ded-e053-2a91aa0a46a1 | 2025-10-19 | Warnings | M017 |
| Clinical Skin Filter Tinted Sunscreen | CLINICAL SKIN FILTER TINTED SUNSCREEN | KRX RESOURCES SDN. BHD. | 22b8856b-671f-def3-e063-6394a90a4ea0 | 2025-10-18 | Warnings | 15FIX9V2JP |
| Clinical Skin Filter Tinted Sunscreen Medium Dark | CLINICAL SKIN FILTER TINTED SUNSCREEN MEDIUM DARK | KRX RESOURCES SDN. BHD. | 22cead37-f862-e859-e063-6394a90a86ce | 2025-10-18 | Warnings | 15FIX9V2JP |
| Krx Aesthetics All Day Glow Sunblocker | KRX AESTHETICS ALL DAY GLOW SUNBLOCKER | KRX RESOURCES SDN. BHD. | 22a60fb9-0fea-92c0-e063-6394a90a088c | 2025-10-18 | Warnings | 15FIX9V2JP |
| Trubrexa | LIDOCAINE AND CAPSAICIN | PHOENIX RX LLC | 3a6500e6-3820-392f-e063-6294a90a769e | 2025-10-17 | Warnings | 98PI200987 |
| CVS Cold and Hot | MENTHOL | CVS Pharmacy | a44cec95-822a-40b6-e053-2995a90ae31c | 2025-10-17 | Warnings | M017 |
| Walgreens Ultra Lubricant | POLYETHYLENE GLYCOL 400, AND PROPYLENE GLYCOL | Walgreens | 21dfe061-4533-2061-e063-6394a90a6e73 | 2025-10-17 | Warnings | 6DC9Q167V3 |
| Lidocaine | LIDOCAINE | PHOENIX RX LLC | 3c69e03c-e176-2c23-e063-6394a90aa41f | 2025-10-17 | Warnings, Adverse reactions | 98PI200987 |
| Sombra Max | SOMBRA MAX | Sombra Cosmetics Inc. | 41623a46-e6e7-907e-e063-6394a90afc4c | 2025-10-17 | Warnings | M017 |
| POMADA DRAGON PAIN RELIEVING | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE | TELEVISA CONSUMER PRODUCTS USA | c283291d-feaa-4f89-8fde-9e3957ea8b9f | 2025-10-17 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.