NDC 87239-1111-01 - Lidoxi
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
- 87239-1111
- Requested NDC
- 87239-1111-01
- Package NDCs from labels
- 87239-1111-1, 87239-1111-01
- Manufacturer
- T&T Pharma Holdings LLC
- Effective date
- 2026-05-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lidoxi - T&T Pharma Holdings LLC | T&T Pharma Holdings LLC | 2026-05-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87239-1111-1 | Lidoxi | 92 g in 1 TUBE, WITH APPLICATOR | OINTMENT | 92 | 1 |
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 |
|---|---|---|---|---|---|---|
| WHITE FLOWER ANALGESIC BALM | CAMPHOR, MENTHOL AND METHYL SALICYLATE | HOE HIN PAK FAH YEOW MANUFACTORY LTD | f3e3b8b5-b12b-49ac-9318-b0c358b136e9 | 2025-10-21 | Warnings | M017 |
| Tri-Vite Drops with Fluoride | ASCORBIC ACID, SODIUM FLUORIDE, VITAMIN A AND VITAMIN D | Method Pharmaceuticals, LLC | 003181d4-5412-4ffe-b99d-880f2010e3ad | 2025-10-21 | Warnings, Adverse reactions | PQ6CK8PD0R |
| Tri-Vite Drops with Fluoride | ASCORBIC ACID, SODIUM FLUORIDE, VITAMIN A AND VITAMIN D | Method Pharmaceuticals, LLC | 5acff360-8d44-44d7-864d-52f213501d03 | 2025-10-21 | Warnings, Adverse reactions | PQ6CK8PD0R |
| LIDOCAINE AND PRILOCAINE | LIDOCAINE AND PRILOCAINE | Bryant Ranch Prepack | 3cd9a055-8b9b-4dff-967b-54023df72e43 | 2025-10-21 | Warnings, Adverse reactions | 98PI200987 |
| LIDOCAINE AND PRILOCAINE | LIDOCAINE AND PRILOCAINE | Bryant Ranch Prepack | 889a8ba8-4058-49e1-8b28-08a3afbf280f | 2025-10-21 | Warnings, Adverse reactions | 98PI200987 |
| Lidocaine | LIDOCAINE | Cardinal Health 107, LLC | eb808fdf-0420-45e9-ad17-8380d49d5c21 | 2025-10-20 | Warnings, Adverse reactions | 98PI200987 |
| Mountain Ice Sports Recovery | MENTHOL | Mountainside Medical Equipment, Inc. | 98638529-3c17-436e-901f-c8aea52bdab6 | 2025-10-20 | Warnings | M017 |
| Lip Clear Lysine Plus | MENTHOL, UNSPECIFIED FORM | Quantum, Inc. | 21a5b4fb-baed-4766-9820-5c6051c14720 | 2025-10-20 | Warnings | M017 |
| Buzz Away Sting Soothe | MENTHOL | Quantum, Inc. | 419e34ea-17b2-ec32-e063-6394a90a603d | 2025-10-20 | Warnings | M017 |
| Family Care Anti-Itch | HYDROCORTISONE | United Exchange Corp. | deb09e89-9794-89a7-e053-2a95a90abdf8 | 2025-10-20 | Warnings | M017 |
| Numbing Cream | MENTHOL | FlexiGo Inc | 41571c8f-332b-f423-e063-6394a90a8897 | 2025-10-20 | Warnings | M017 |
| Soothing Nerve Therapy | MENTHOL | Wise Consumer Products | 40829d6b-5005-7ec9-e063-6294a90a970e | 2025-10-20 | Warnings | M017 |
| Numbing Cream | MENTHOL | FlexiGo Inc | 4146fd51-b18c-393d-e063-6294a90a4d9a | 2025-10-20 | Warnings | M017 |
| Lidocaine 4% Maximum OTC Strength | LIDOCAINE | Cardinal Health 107, LLC | 975031df-d46d-4098-b1c0-1c0c92b41995 | 2025-10-20 | Warnings | M017 98PI200987 |
| Cortizone 10 Intensive Healing | HYDROCORTISONE | Chattem, Inc. | bb3d1a3e-4c0c-4694-9c05-80152dd9bd1c | 2025-10-20 | Warnings | M017 |
| Sting relief pad | BENZOCAINE, ALCOHOL | Guangdong Comfort Medical Products Co., Ltd. | 6e905065-10a9-1ded-e053-2a91aa0a46a1 | 2025-10-19 | Warnings | M017 |
| Trubrexa | LIDOCAINE AND CAPSAICIN | PHOENIX RX LLC | 3a6500e6-3820-392f-e063-6294a90a769e | 2025-10-17 | Warnings | 98PI200987 |
| CVS Cold and Hot | MENTHOL | CVS Pharmacy | a44cec95-822a-40b6-e053-2995a90ae31c | 2025-10-17 | Warnings | M017 |
| Lidocaine | LIDOCAINE | PHOENIX RX LLC | 3c69e03c-e176-2c23-e063-6394a90aa41f | 2025-10-17 | Warnings, Adverse reactions | 98PI200987 |
| Sombra Max | SOMBRA MAX | Sombra Cosmetics Inc. | 41623a46-e6e7-907e-e063-6394a90afc4c | 2025-10-17 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.