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 |
|---|---|---|---|---|---|---|
| Addiclenz | ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYLPARABEN, PROPYLPARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUM, ARSENICUM ALBUM, BETA VULGARIS, BISPHENOL A, BOLDO, CHELIDONIUM MAJUS, COBALTUM METALLICUM, CUPRUM METALLICUM, GLYPHOSATE, IODIUM, LYCOPODIUM CLAVATUM, PETROSELINUM SATIVUM, PHOSPHORICUM ACIDUM, SELENIUM METALLICUM, TARAXACUM OFFICINALE, ZINCUM METALLICUM | Deseret Biologicals, Inc. | 25036c26-1c21-4e5a-b4db-b8e177458341 | 2025-03-11 | Warnings | 15FIX9V2JP |
| Arctic Blast Pain Releiving | MENTHOL, CAMPHOR (SYNTHETIC) | Nutriomo Labs Pte, Ltd | d5e7d26d-4f63-4b7b-a173-fe3a794c8459 | 2025-03-10 | Warnings | M017 |
| Anti Itch | WALGREEN | Walgreens | 30014ff0-2519-4031-e063-6394a90ae07b | 2025-03-10 | Warnings | M017 |
| 5% Signature Numb cream | 5% LIDOCAINE | Shengnan (Guangzhou) Cosmetics Co., LTD | 3008bbeb-abba-5cdb-e063-6294a90ae483 | 2025-03-10 | Warnings | 98PI200987 |
| Anti Itch | ANTI ITCH | Neilmed Pharmaceuticals Inc. | 2fa74baf-e3d2-e099-e063-6394a90a1bae | 2025-03-06 | Warnings | M017 |
| Thunder Fck Male Genital Desensitizer | BENZOCAINE | PRODUCT MAX GROUP INC | 93188a42-0d3c-4159-bdc7-bbc5ec5c6744 | 2025-03-06 | Warnings | M017 |
| Body Action Climax Guard Delay | BENZOCAINE | PRODUCT MAX GROUP INC | f88e0b42-974e-4f46-a93b-34b06320770a | 2025-03-06 | Warnings | M017 |
| Curist Hemorrhoid Fissure Relief | LIDOCAINE | Little Pharma, Inc | 2fb02b00-acdb-5184-e063-6294a90ae1c8 | 2025-03-06 | Warnings | 98PI200987 PDC6A3C0OX |
| XENCARE INFLAMAX NATURAL TOPICAL PAIN | MENTHOL, CAPSAICIN | Xenex Laboratories Inc. | 25b9621b-3c16-3cb9-e063-6294a90ab598 | 2025-03-06 | Warnings | M017 |
| Pain Relieving Cream | CAMPHOR AND MENTHOL | PAIN WIZARD LIMITED LIABILITY COMPANY | 1cd37b69-2cfb-130d-e063-6394a90af50b | 2025-03-06 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE | Walgreens Co. | c22bba5c-bb6f-494e-987a-f6e36c1b4893 | 2025-03-06 | Warnings | M017 |
| Redicare Burn Gel | REDICARE BURN GEL | Redicare LLC | 947ac362-acfb-3508-e053-2a95a90a2873 | 2025-03-05 | Warnings | M017 |
| 5% Signature Numb cream | 5% SIGNATURE | Shengnan (Guangzhou) Cosmetics Co., LTD | 2f80abc0-49d8-968d-e063-6294a90a555b | 2025-03-04 | Warnings | 98PI200987 |
| Thera Plus Hydrocortisone Maximum Strength | HYDROCORTISONE | FOURSTAR GROUP USA, INC. | c2bc8f0c-38ea-4124-bc51-bf22e6751a92 | 2025-03-04 | Warnings | M017 |
| Thera Plus Eczema Hydrocortisone Anti Itch | HYDROCORTISONE | Fourstar Group USA, Inc. | 7c72217b-db9a-4573-9f14-4c11528fa452 | 2025-03-04 | Warnings | M017 |
| Thera Plus Hemorrhoidal | GLYCERIN, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE | FOURSTAR GROUP USA, INC. | 87143a7a-7b2d-4b67-afda-2355697e7300 | 2025-03-04 | Warnings | PDC6A3C0OX |
| Thera Plus Maximum Strength Hydrocortisone | HYDROCORTISONE | Fourstar Group USA, Inc. | fb89dca6-c0c0-4092-b3f5-e59c956c3d6c | 2025-03-04 | Warnings | M017 |
| 5% Dr.care Numb cream | LIDOCAINE | Shengnan (Guangzhou) Cosmetics Co., LTD | 2f905d76-ef9c-c844-e063-6394a90a4dc9 | 2025-03-04 | Warnings | 98PI200987 |
| MINERAL TINTED SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BOTANICAL SCIENCE, INC. | 2f9e2252-fb54-363f-e063-6294a90aa7c9 | 2025-03-04 | Warnings | 15FIX9V2JP |
| Peppermint soothing cream | CAMPHORIC ACID, MENTHOL, UNSPECIFIED FORM, BORNEOL | Henan Lijitang Medical Technology Co., Ltd. | 2f6bc332-3006-710d-e063-6394a90acea5 | 2025-03-03 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.