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 |
|---|---|---|---|---|---|---|
| A and E Deep Throat Desensitizing SprayPeppermint | ORAL NUMBING SPRAY MINT | Phe Inc | 4355e0d0-1222-d594-e063-6294a90abb29 | 2025-11-11 | Warnings | M017 |
| DermaNumb Analgesic | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 0ea46890-45c3-4732-bc47-227f7c67daf1 | 2025-11-11 | Warnings | M017 |
| Derma Numb Pain Relief | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 710991ae-8f82-4893-93a7-0ef3f815d132 | 2025-11-11 | Warnings | M017 |
| Essential Defense Mineral Shield Broad Spectrum SPF 32 Sunscreen TINTED | TITANIUM DIOXIDE AND ZINC OXIDE | Allergan, Inc. | 279a5214-79b2-44e9-b003-378d0b992395 | 2025-11-11 | Warnings | 15FIX9V2JP |
| HYDROCORTISONE | HYDROCORTISONE | Encube Ethicals, Inc. | 969cd576-82d3-4662-bbc1-3587a1f6a564 | 2025-11-10 | Warnings | M017 |
| Lidocaine | LIDOCAINE | Bryant Ranch Prepack | 4e679a0d-df82-435f-ad46-c871f3c76dfb | 2025-11-10 | Warnings, Adverse reactions | 98PI200987 |
| Jelcaine Sterile | LIDOCAINE HCL JELLY USP, 2% | Brookfield Pharmaceuticals, LLC | 1a39d1de-7aa2-3068-e063-6394a90aed85 | 2025-11-10 | Warnings | M017 |
| Hush Anesthetic | LIDOCAINE | HUSH Anesthetic | c6e86a0f-6f9b-45b7-86ce-0bb1c198061a | 2025-11-10 | Warnings | M017 98PI200987 |
| Hush Anesthetic | LIDOCAINE | HUSH Anesthetic | 97ae1993-7268-4b7f-92e2-6004337d5650 | 2025-11-10 | Warnings | M017 98PI200987 |
| MENTHOL AND METHYL SALICYLATE | ELECTRIC MEDICATED BALM ULTRA STRENGTH | FEI FAH MEDICAL MANUFACTURING PTE LTD | 91e6d3b9-25bb-4015-9d96-bd27f93e5ada | 2025-11-10 | Warnings | M017 |
| buttah Tinted Mineral Sunscreen SPF-30 | TITANIUM DIOXIDE, ZINC OXIDE | Buttah Enterprises, LLC. | 43458152-0775-dd9c-e063-6394a90a6140 | 2025-11-10 | Warnings | 15FIX9V2JP |
| E MEI SHAN MEDICATED | CAMPHOR, MENTHOL | Zhejiang Dingtai Pharmaceutical Co., Ltd | bda1e7c1-42df-4126-a512-80f843b07fd0 | 2025-11-10 | Warnings | M017 |
| EXTRA STRENGTH HUA TUO PAIN RELIEVING | CAMPHOR AND MENTHOL | Zhejiang Dingtai Pharmaceutical Co., Ltd | 9850754b-ac94-4ec6-b75a-8096e5ac9456 | 2025-11-10 | Warnings, Adverse reactions | M017 |
| TONG FENG DING PAIN RELIEF | CAMPHOR AND MENTHOL | Zhejiang Dingtai Pharmaceutical Co., Ltd | fe87b864-b3ee-4a4b-8e5a-e1ee6493de0d | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Solstice Pain Relieving | CAMPHOR, MENTHOL, METHYL SALICYLATE | MADISON ONE ACME INC | 5ef90782-8201-47d1-b57f-f032d4c9b06a | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Solstice Pain Relieving | CAMPHOR, MENTHOL, METHYL SALICYLATE | MADISON ONE ACME INC | 1388ab3a-c26f-427d-898d-0d88411a5fba | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Solstice Capsaicin Patch Hot | CAPSAICIN | MADISON ONE ACME INC | f74db6e0-853a-4eb3-a4b5-9da2cd3d95cf | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Lung Choy Shung Pain Relief Liquid | MENTHOL AND CAMPHOR | MADISON ONE ACME INC | 4842c6ec-7823-4f6b-afc4-258fce2c2391 | 2025-11-10 | Warnings, Adverse reactions | M017 |
| 701 DIEDA ZHENGTONG YAOGAO MEDICATED | CAMPHOR AND MENTHOL | MADISON ONE ACME INC | 115041ff-5046-4ca4-b54b-5652037e74bd | 2025-11-10 | Warnings, Adverse reactions | M017 |
| EXTRA STRENGTH HUA TUO PAIN RELIEF | CAMPHOR AND MENTHOL | MADISON ONE ACME INC | 0f269a41-4b56-4e22-b9cb-17d99bf76a57 | 2025-11-10 | Warnings, Adverse reactions | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.