NDC 50488-1001-01 - Terocin
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
- 50488-1001
- Requested NDC
- 50488-1001-01
- Package NDCs from labels
- 50488-1001-1, 50488-1001-01
- Manufacturer
- Alexso, Inc
- Effective date
- 2026-10-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Terocin - Alexso, Inc | Alexso, Inc | 2026-10-19 | HUMAN OTC DRUG LABEL |
| Terocin Patch | Preferred Pharmaceuticals, Inc. | 2026-09-30 | HUMAN OTC DRUG LABEL |
| Terocin - ASCLEMED USA INC. | ASCLEMED USA INC. DBA ENOVACHEM | ASCLEMED USA INC. | ASCLEMED USA INC. DBA ENOVACHEM | 2026-05-05 | HUMAN OTC DRUG LABEL |
| Terocin - Quality Care Products LLC | Quality Care Products LLC | 2023-12-21 | HUMAN OTC DRUG LABEL |
| Terocin - A-S Medication Solutions | A-S Medication Solutions | 2021-05-26 | HUMAN OTC DRUG LABEL |
| Terocin Patch | NuCare Pharmaceuticals,Inc. | 2021-02-22 | HUMAN OTC DRUG LABEL |
| Terocin - Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2020-12-11 | HUMAN OTC DRUG LABEL |
| NOpioid-LMC - Skya Health, LLC | Skya Health, LLC | 2020-10-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Terocin - A-S Medication Solutions | A-S Medication Solutions | 2020-01-18 | HUMAN OTC DRUG LABEL |
| TEROCIN - DirectRX | DirectRX | 2019-04-23 | HUMAN OTC DRUG LABEL |
| Terocin - medsource pharmaceuticals | medsource pharmaceuticals | 2018-12-20 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50488-1001-1 | Terocin | 2 in 1 BOX | PATCH | 2 | 6 | |
| 50488-1001-1 | Terocin | 5 in 1 POUCH | PATCH | 5 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50488-1001 | TEROCIN (LIDOCAINE, MENTHOL) PATCH [ALEXSO, INC] | 6 | Current NDC, Legacy NDC, 2 package rows | 20241208_100ceb76-8ebe-437b-a8de-37cc76ece9bb.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50488-1001-1 | EA - Each | 50488-1001 | ee8e93c8-555b-43a2-b4b0-b07e6026efed | 1 | 2013-08-02 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Priia Tinted Mineral Sunscreen and Primer | TITANIUM DIOXIDE, ZINC OXIDE | Priia Cosmetics Inc | 5c4219ac-d65f-43a5-8ec4-8732b9b344cf | 2025-01-13 | Warnings | 15FIX9V2JP |
| Brush and Go Oily Problematic Skin | TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE | Noon Aesthetics M.R. Ltd | b4295453-f193-4bed-be5b-efcd91772107 | 2025-01-13 | Warnings | 15FIX9V2JP |
| Priia Tinted Mineral Sunscreen and Primer | TITANIUM DIOXIDE, ZINC OXIDE | Priia Cosmetics Inc | b2addf27-9139-48b4-85e6-618f4b5311cc | 2025-01-13 | Warnings | 15FIX9V2JP |
| Arthritis Hot | MENTHOL AND METHYL SALICYLATE | Chattem, Inc. | cc57b9b6-8ba5-4ff3-a5df-97d8f5b1bebd | 2025-01-13 | Warnings | L7T10EIP3A |
| SUN PROTECT LIP BALM SPF 30 | ZINC OXIDE AND TITANIUM DIOXIDE | Stream2Sea, LLC | 21386652-b952-48be-b077-1acecc7f0eb0 | 2025-01-12 | Warnings | 15FIX9V2JP |
| Re-Lieved Lidocaine Patch | LIDOCAINE PATCH 4% | Transfer Technology | 00b40dda-53ad-0458-e063-6394a90aa835 | 2025-01-11 | Warnings | 98PI200987 |
| Re-Lieved Lidocaine Patch | LIDOCAINE PATCH 4% | Transfer Technology | 00b47eb7-6b43-d9e2-e063-6294a90a9a38 | 2025-01-11 | Warnings | 98PI200987 |
| Re-Lieved 4% Lidocaine Fabric Tape | LIDOCAINE 4% FABRIC TAPE | Transfer Technology | e9a894b0-54f2-707e-e053-2a95a90a0f0d | 2025-01-11 | Warnings | 98PI200987 |
| Lidocaine 5% | LIDOCAINE 5% | Asclemed USA, Inc. | 1dca5b81-72a9-4969-8552-d43091f72aab | 2025-01-10 | Warnings, Adverse reactions | 98PI200987 |
| Dermaroller Anhydrous Sunscreen SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Owen Biosciences, Inc. | 04e82f1b-c893-4795-b7a9-0523e3ec7552 | 2025-01-10 | Warnings | 15FIX9V2JP |
| LABOFLEX Lidocaine Pain Relieving Patch | LIDOCAINE 4% | Laboflex, Inc. | 31995f31-c272-afdb-e063-6294a90af3f9 | 2025-01-10 | Warnings | 98PI200987 |
| Kanka Triple Action | BENZOCAINE AND MENTHOL, UNSPECIFIED FORM | Blistex Inc. | 078fcdab-38a1-4a9a-bdd3-e17446591ea8 | 2025-01-09 | Warnings | L7T10EIP3A |
| Protect Tinted Mineral Sunscreen Broad Spectrum SPF 30 | TITANIUM DIOXIDE AND ZINC OXIDE | NEW SEASON DERMATOLOGY, PLLC | fecd72a3-c7e5-3dfa-e053-6394a90a7357 | 2025-01-09 | Warnings | 15FIX9V2JP |
| STERILE WATER | STERILE WATER | HF Acquisition Co. LLC, DBA HealthFirst | 74ed2a6f-824c-a1ff-e053-2a91aa0a57c0 | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 77bd3c0f-f4ab-7cfa-e053-2a91aa0a1b83 | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 7610bf80-61b7-982f-e053-2a91aa0ac1bb | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| ECLIPSE SPF 50 PERFECTINT BEIGE | TITANIUM DIOXIDE, ZINC OXIDE | SCIENCE OF SKINCARE LLC | b69dda25-372f-15d9-e053-2995a90a8d3e | 2025-01-09 | Warnings | 15FIX9V2JP |
| Extreme Protect SPF 40 All Shades | ZINC OXIDE, TITANIUM DIOXIDE | Science of Skincare, LLC. | b69db78b-5f0e-8ca2-e053-2a95a90ac88c | 2025-01-09 | Warnings | 15FIX9V2JP |
| ECLIPSE SPF 50 ALL SHADES | TITANIUM DIOXIDE, ZINC OXIDE | SCIENCE OF SKINCARE LLC | 49df51e6-be9a-41be-b3e1-bfc062aaceaa | 2025-01-09 | Warnings | 15FIX9V2JP |
| PAIN-X | MENTHOL | OL PHARMA TECH,LLC | b22bb19a-14e5-3d32-e053-2a95a90ae520 | 2025-01-09 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.