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LIDODERM® (LIDOCAINE PATCH 5%)

LIDODERM is indicated for relief of pain associated with post-herpetic neuralgia

LIDODERM (lidocaine patch 5%) is comprised of an adhesive material containing 5% lidocaine, which is applied to a non-woven polyester felt backing and covered with a polyethylene terephthalate (PET) film release liner. 

Lidoderm (lidocaine patch 5%) Patient Information

Lidoderm Prescribing Information

Lidoderm Prescribing Information (PDF)

TPU Pharma_Lidoderm Prescribing Information (pdf)Download

Lidoderm Package Insert

Lidoderm USPI_220914 (pdf)Download

LIDODERM® (LIDOCAINE PATCH 5%)


Launched in 1999, Lidoderm was the first prescription, topical, hydrogel patch approved in the United States for post-herpetic neuralgia (PHN). Lidoderm provides analgesia (without anesthesia) directly to the affected nerves.

LIDODERM is indicated for relief of pain associated with post-herpetic neuralgia.  


Important Safety Information

  • You should not use this product if you are sensitive to local anesthetics such as lidocaine, or to any of the other ingredients in LIDODERM.
  • Even a used  LIDODERM patch contains a large amount of lidocaine. A small child or a pet could suffer serious adverse effects from chewing or swallowing a new or used LIDODERM patch. Store and dispose of patches out of the reach of children, pets, and others. Never reuse a patch.
  • LIDODERM patches should be worn for no more than 12 hours a day. Applying the patches for a longer time or using more than 3 patches could cause serious reactions.
  • LIDODERM should be applied only to intact skin





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