Active Ingredient
Lidocaine 4%
Purpose
Topical Analgesic
Lidocaine 4%
Topical Analgesic
For the temporary relief of pain
For external use only
If you are allergic to any ingredient in Re-Lieved Lidocaine Patch, on open wounds or damaged irritated skin.
Ask your doctor or pharmacist before use if you are using blood thining medication, steroids, or non-steroidal anti-inflammatory drugs (NSAIDS)
When using this product
Stop use or ask a doctor if
If pregnant or breastfeeding ask a physican before use.
Keep out of reach of children. If put in mouth, get medical help or contact a poison control center right away.
Directions adults and children 12 years or older
Other information
Inactive ingredients: Acrylic adhesive, polyethylene foam
| Class | Version | Type | Effective |
|---|---|---|---|
| LIDOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71662-000-01 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-9346-d83d-e063-dadaa90ab31f | Re-Lieved Lidocaine 4% Patch |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71662-000-01 | Re-Lieved Lidocaine Patch | 116 cm2 in 1 POUCH | PATCH | 116 | 6 |
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71662-000-01 | EA - Each | 71662-000 | 00a56070-24c6-4880-bf29-e99cda564ab2 | 1 | 2022-09-12 |
| 71662-000-20 | EA - Each | 71662-000 | 958bdf69-3945-4f07-b11f-6fc74a4259d2 | 1 | 2023-12-05 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 71662-000 | 71662-000-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) | 1PEZ3NLY6I | IACT |
| LIDOCAINE | 98PI200987 | ACTIB |
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.
Adverse event summaries are temporarily unavailable. Other product information remains available.