Lidocaine Hydrochloride Liquid
FDA Label NDC 0924-0934

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Acme United Corporation for the product Lidocaine Hydrochloride (NDC 0924-0934). 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 other, active ingredients, purpose, use, warnings, do not use, otc - stop use, 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

Other

Drug Facts

Active Ingredients

Lidocaine HCl 2.0%

Purpose

Topical pain relief

Use

Temporarily relieves pain associated with minor burns.

Warnings

For external use only.

Do Not Use

  • in eyes, if contact occurs rinse thoroughly with water
  • in large quantities, particularly over raw or blistered areas

Otc - Stop Use

Stop use and ask a doctor if condition worsens, or persists for more than 7 days or clears up and returns

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away

Directions

  • adults and children 2 years of age and older: spray an even layer of burn spray over affected area not more than 3-4 times daily
  • children under 2 years of age: consult a doctor

Inactive Ingredients

aloe vera, diazolidinyl urea, propylene glycol, purified water
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