Alcohol Prep Pad
FDA Label NDC 36769-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by B�ttner-frank Gmbh Arzt- Und Krankenhausbedarf - Krankenpflege Und Einmalartikel for the product Alcohol Prep Pad (NDC 36769-001). 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, inactive ingredient, purpose, use, keep out of reach of children, directions, warnings, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Isopropyl Alcohol 70% v/v

Inactive Ingredient

Purified Water

Purpose

Antiseptic

Use

For Preparation of skin prior to injection

Keep Out Of Reach Of Children

Keep out of reach of children

Directions

Wipe Injection site vigorously and discard

Warnings

For external use only.  Flammable, keep away from fire or flame. 

Do not use

  • With electrocautary procedures
    • In the eyes.  
      • Stop use if irritation or redness develop.  If the condition persists for more than 72 hours consult a doctor.
      If swallowed, get medical help or contact a Poison Control Center right away.

Package Label

Latex Free Alcohol Prep Pad  Antiseptic

Buttner-Frank GmbH  Am Wolfsmantel 9-11  91058 Erlangen, Germany

Contents: 1 Pad  LOT_____________ EXP _________________  NDC _____________________

Tear Here

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