Alcohol Prep Pad
FDA Label NDC 43128-050

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ndc National Distribution & Contracting, Inc. for the product Alcohol Prep Pad (NDC 43128-050). 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 ingredients, purpose, use, warnings, otc - do not use, otc - stop use, otc - 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

Active Ingredients

Isopropyl Alcohol 70%

Purpose

Antiseptic Cleanser

Use

For Preparation of Skin prior to an injection

Warnings

Warnings

  • For External Use Only
  • Flammable, Keep away from fire or flame

Otc - Do Not Use

Do Not Use

  • with electrocautery procedures
  • In the Eyes. If contact occurs, flush eyes with water

Otc - Stop Use

Stop Use

If irritation and redness develop. 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 injection site vigorously and discard.

Storage And Handling

Other Information

Store at Room Temperature 15 - 30 C (59 - 86 F)

Inactive Ingredient

Inactive Ingredient

purified water

Principal Display Panel - 100 Pouch Box Label

REF: P902050

Sterile

Alcohol
Prep Pads

Large (1.75 IN × 3.5 IN)

For Professional and Hospital Use

Sterile unless package is opened or damaged.
Do not resterilize.

Pro
Advantage ®
by NDC

10 boxes/case | 100/box

Principal Display Panel (100 Pouch Box Label)

Principal Display Panel (100 Pouch Box Label)

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