Active Ingredient
Lidocaine 4%
Re-lieved Lidocaine Patch
FDA Label NDC 71662-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Transfer Technology for the product Re-lieved Lidocaine Patch (NDC 71662-000). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, otc - when using, pregnancy, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical Analgesic
Use
For the temporary relief of pain
Warnings
For external use only
Do Not Use
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)
Otc - When Using
When using this product
- do not use other topical products
- avoid contact with eyes or mucous membranes
- keep away from excessive heat
Pregnancy
If pregnant or breastfeeding ask a physican before use.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If put in mouth, get medical help or contact a poison control center right away.
Other Safety Information
Other information
- Store at room temperature
- Do not exceed 100 o Fahrenheit 38 o Celsius
- For easier removal of patch apply rubbing alcohol or baby oil to adhesive edge
Inactive Ingredient
Inactive ingredients: Acrylic adhesive, polyethylene foam
Re-Lieved Lidocaine 4% Patch
Re-lieved Lidocaine Box (Relievedbagdesign8.17front)
Drug Facts Panel
Drug Facts Panel (Relievedbagdesign8.17back)
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