Alcohol Prep Pad-large Swab
FDA Label NDC 72727-0001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Global Biomedical Technologies, Llc for the product Alcohol Prep Pad-large (NDC 72727-0001). 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, purpose, use, warnings:, otc - 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 Ingredient

70% isopropyl alcohol, saturated prep pads.

Purpose

Bandage releasing agent

Use

To release bandage from the skin

Warnings:

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

Otc - Do Not Use

Do Not Use with electrocautery procedures or in the eyes. If contact occurs, flush eyes with water.

Otc - Stop Use

Stop Use if irritation and redness develops. If condition persists consult your health care practitioner.

Otc - Keep Out Of Reach Of Children

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

Directions:

Wipe over bandage for several seconds (to release bandage from the skin) vigorously and then discard. Store at room temperature (59° - 86°F).

Inactive Ingredient

purified water.

Principal Display Panel - Carton Label

Comfort
Release®

Sticks when you need it.
Releases when you don't.

FOR SENSITIVE SKIN

  • Easy to apply
  • Water resistant
  • Breathable
  • Long lasting
  • Painless release

    • 10 Comfort Release® Bandages

    Bandages // 2" x 4" (5.1 cm x 10.2 cm)

    Includes 20 Alcohol Prep Pads for Removal

    NDC 72727-0001-2

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