Medi-first Burn Gel
FDA Label NDC 47682-477

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Unifirst First Aid Corporation for the product Medi-first Burn (NDC 47682-477). 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 ingredient (in each gram), purpose, uses, warnings, do not use, when using this product, stop use ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient (In Each Gram)

Lidocaine HCI 2.0%

Purpose

Topical analgesic

Uses

For the temporary relief of pain associated with minor burns.

Warnings

For external use only.

Do Not Use

  • in large quantities, particularly over raw or blistered areas

Stop Use Ask A Doctor If

  • condition worsens
  • symptoms persist for more than 7 days or clears up and occurs again within a few days

Otc - Keep Out Of Reach Of Children

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

Directions

  • adults & children 2 years and older: apply to affected area not more than 3 to 4 times daily
  • children under 2: consult a doctor

Inactive Ingredients

aloe vera, carbomer, germaben II, propylene glycol, purified water, menthol, triethanolamine, vitamin E acetate

Questions?

Call 1-800-634-7680

Mfg. for Medique Products, 17080 Alico Commerce Ct., Ste 1, Fort Myers, FL 33967

Package Label.Principal Display Panel

MF Burn Gel Label

Medi-First ®

Burn Gel

Product # 47769

NET CONTENTS: 6 Units of 1/8 oz

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