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 |
|---|---|---|---|---|---|---|
| Blue Lizard Sheer Face SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | baed8202-21fd-3a43-e053-2a95a90ada32 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Sensitive Face Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Crown Laboratories | 88dbd396-8955-271e-e053-2995a90a0a7a | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Baby SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 9d237fb7-4f5f-521d-e053-2a95a90a9734 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Sarna | PRAMOXINE HYDROCHLORIDE | Crown Laboratories | 19b0ce1b-e147-01a1-e063-6394a90af808 | 2026-01-12 | Warnings | M017 |
| Sarna | PRAMOXINE HYDROCHLORIDE, MENTHOL | Crown Laboratories, Inc | 19c41e75-a654-90cf-e063-6394a90a7e97 | 2026-01-12 | Warnings | M017 |
| Blue Lizard Sensitive Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 1e4d49f4-9e77-48b5-bce5-ff04ed885a0f | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Baby SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 32d6e04a-fa30-ba48-e063-6394a90a1bbf | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Kids SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 2f780daa-4c91-5a68-e063-6394a90afd41 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Sport SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 2f3844d8-0367-aad9-e063-6294a90a1fce | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Sheer Face SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 30cd79da-2f25-a42a-e063-6394a90a8332 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | HY-VEE, INC | 48350b54-8d9a-48c4-e063-6394a90ac040 | 2026-01-12 | Warnings | M017 |
| LidoPlus Pain Relief | LIDOCAINE HYDROCHLORIDE | Centura Pharmaceuticals, Inc | 07bacc6c-60a6-4297-8663-904a22bdc040 | 2026-01-12 | Warnings | M017 |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f1efb51c-5217-4cb2-e053-2a95a90a7f95 | 2026-01-12 | Warnings | M017 |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f2277e27-868b-57ef-e053-2a95a90abf28 | 2026-01-12 | Warnings | M017 |
| Urea 20 | UREA | AvPAK | e994fa05-a457-2555-e053-2a95a90ae83b | 2026-01-12 | Warnings | 8W8T17847W |
| ACCOJE PROTECTIVE AIR-FIT MINERAL SUNSCREEN | TITAMIUN DIOXIDE, ZINC OXIDE | UCL Co., Ltd. | 4837b4f6-ada9-801a-e063-6294a90a8547 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Intellishade Original SPF 45 | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE | Revision, LLC | e213a681-eb22-69c0-e053-2995a90a899e | 2026-01-12 | Warnings | 15FIX9V2JP |
| BLT 3 | TETRACAINE | CENTURA PHARMACEUTICALS INC | 401a0d22-1181-02ac-e054-00144ff88e88 | 2026-01-12 | Warnings | M017 |
| Sting Relief Prep Pad | BENZOCAINE | NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | 0c901f64-6890-45c0-9ca7-ee9de87903c4 | 2026-01-12 | Warnings | M017 |
| Goodsense Oral Pain Relief | BENZOCAINE | Geiss, Destin and Dunn, Inc. | eb461b70-d10f-4e11-8374-e43713f3504d | 2026-01-12 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.