Medifirst Hydrogen Peroxide Spray
FDA Label NDC 47682-257

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 Medifirst Hydrogen Peroxide (NDC 47682-257). 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, uses, warnings, do not use, keep out of reach of children., directions, 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

Hydrogen Peroxide 3.0%

Purpose

First Aid Antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only.

Do Not Use

  • near eyes or mucous membranes
  • on deep or puncture wounds, animal bites, or serious burns consult a doctor

Keep Out Of Reach Of Children.

Caution

  • not for use on large areas of the body
  • if redness, irritation, swelling or pain persists or increases, discontinue use and consult a physician

Directions

  • spray over affected area
  • if bandaged, let dry first
  • not to be used on children under 12 years of age

Inactive Ingredient

purified water

Questions Or Comments?

1-800-634-7680

Principal Display Panel - Bottle Label

MEDI-FIRST ®

Hydrogen Peroxide

Pump Spray

Antiseptic

  • Treats minor cuts, scrapes and abrasion
  • Helps prevent infection

    • 2 FL OZ (59.1ML)

    Med0y-0001-02 (Med0y 0001 02)

    Med0y-0001-02 (Med0y 0001 02)

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