NDC 50488-1025-01 - Capsaicin
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
- 50488-1025
- Requested NDC
- 50488-1025-01
- Package NDCs from labels
- 50488-1025-1, 50488-1025-5, 50488-1025-2, 50488-1025-01
- Manufacturer
- Alexso, Inc
- Effective date
- 2024-12-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Capsaicin - Alexso, Inc | Alexso, Inc | 2024-12-06 | HUMAN OTC DRUG LABEL |
| CapsFenac Pak - SA3, LLC | SA3, LLC | 2020-01-24 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50488-1025-1 | Capsaicin | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 50488-1025-1 | Capsaicin | 120 g in 1 TUBE | CREAM | 120 | 6 | |
| 50488-1025-2 | Capsaicin | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 50488-1025-2 | Capsaicin | 25 g in 1 TUBE | CREAM | 25 | 6 | |
| 50488-1025-5 | Capsaicin | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 50488-1025-5 | Capsaicin | 50 g in 1 TUBE | CREAM | 50 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50488-1025 | CAPSAICIN CREAM [ALEXSO, INC] | 6 | Current NDC, Legacy NDC, 6 package rows | 20241208_433da27d-04fb-481a-bbb0-874bb72c806a.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50488-1025-1 | GM - Gram | 50488-1025 | d17846c1-27c2-4422-951e-81c30af4e47b | 1 | 2018-11-06 |
| 50488-1025-2 | GM - Gram | 50488-1025 | 990eddfb-a7a5-4493-b6e9-371140c2fd9d | 1 | 2019-10-07 |
| 50488-1025-5 | GM - Gram | 50488-1025 | 9795f0e9-7933-4d81-9bc2-c7b3efa42c38 | 1 | 2018-11-06 |
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 |
|---|---|---|---|---|---|---|
| ARTHRITIS PAIN RELIEVING | DICLOFENAC SODIUM | Meijer, Inc. | 5cc570c6-2585-4d1a-9352-b1161458af9a | 2025-11-17 | Warnings | QTG126297Q |
| Smart Care Barbie HAND SANITIZER COTTON CANDY SCENT | ETHYL ALCOHOL | Ashtel Studios, Inc. | 09a7ea30-9a07-4aca-87d5-1c56a210975d | 2025-11-16 | Warnings | 3K9958V90M |
| Antifungal cream | ANTIFUNGAL CREAM | Guangzhou Guoyoumi Biotechnology Co Ltd | 43a5b3c8-3b99-b113-e063-6394a90a9aff | 2025-11-15 | Warnings | PDC6A3C0OX |
| Blue-Emu Thrive Pain Relief Cream | TRIPELENNAMINE 0.5% | Kingsway Pharmaceuticals dba NFI, LLC | a4ba6787-c99b-4bf2-9f8f-e923ef976212 | 2025-11-14 | Warnings | M017 |
| CVS Cooling Patch | MENTHOL | CVS Pharmacy | 42d97e29-f32d-a31b-e063-6394a90a88d8 | 2025-11-14 | Warnings | M017 |
| Lidocaine | LIDOCAINE | Marlex Pharmaceuticals Inc | 4de2bc60-dc4a-4417-984f-eabab0e926a6 | 2025-11-14 | Warnings | M017 |
| Diclofenac Sodium Delayed Release | DICLOFENAC SODIUM | PHOENIX RX LLC | 41472cca-278b-934b-e063-6294a90aaf5d | 2025-11-14 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| Diclofenac Sodium | DICLOFENAC SODIUM | PHOENIX RX LLC | 4382cc15-8978-4f3b-e063-6394a90a9ecb | 2025-11-14 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| EXTREME EMU | MENTHOL, METHYL SALICYLATE | Renu Laboratories, LLC | 4393b57b-1e70-b8dd-e063-6294a90ae748 | 2025-11-14 | Warnings | M017 |
| 4x Medicated Toothache and Gum Cream | BENZOCAINE | Kroger | a8c5090a-24f9-4e73-e053-2a95a90acca0 | 2025-11-14 | Warnings | M017 |
| PM Toothache Relief | BENZOCAINE | CVS | 0a5a8cd0-d680-8a0f-e063-6294a90aa65c | 2025-11-14 | Warnings | M017 |
| PM Toothache Relief | BENZOCAINE | Walgreens | e816f742-fba9-3c12-e053-2a95a90a192f | 2025-11-14 | Warnings | M017 |
| 4x Medicated Toothache and Gum Cream | BENZOCAINE | Walgreens | a71c2092-4ece-b82e-e053-2995a90ac933 | 2025-11-14 | Warnings | M017 |
| After Bite Outdoor | DIPHENHYDRAMINE HCL | Tender Corporation d/b/a Adventure Ready Brands | 22b891a9-6386-dee1-e063-6394a90a5c2f | 2025-11-14 | Warnings | M017 |
| QR PAIN | ANALGESIC | MARYHELENE ENTERPRISES INC | 8f8f53e3-fe31-e7b5-e053-2995a90a710d | 2025-11-14 | Warnings | M017 |
| QR PAIN | ANALGESIC | MARYHELENE ENTERPRISES INC | 9984a510-30be-4013-e053-2995a90a841e | 2025-11-14 | Warnings | M017 |
| Mist | ALCOHOL | Derma Glove | 4513f6b9-ceac-415d-a1af-1f7585c5989e | 2025-11-14 | Warnings | 3K9958V90M |
| Hand Recovery | ALCOHOL | Derma Glove | 90058ba8-e55d-4318-9fc5-8f0d25dfdd99 | 2025-11-14 | Warnings | 3K9958V90M |
| Anti-Itch Cream | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE | Kroger | 3f881349-fcdd-e276-e063-6394a90ae49e | 2025-11-13 | Warnings | M017 |
| Rapid Relief | PLANTAR FASCIITIS PAIN RELIEF LIDOCAINE 4% MENTHOL 1% | RAPID AID VIET NAM COMPANY LIMITED | 434cb8b2-a996-5360-e063-6394a90ada03 | 2025-11-13 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.