Alcohol Prep Pads Swab
FDA Label NDC 63517-500

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health for the product Alcohol Prep Pads (NDC 63517-500). 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, uses, warnings, do not use, stop use and ask doctor if, caution, 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

Active Ingredients

Isopropyl Alcohol USP, 70% v/v

Purpose

Antiseptic

Uses

For preparation of skin prior to injection

Warnings

For external use only

Flammable. Keep away from fire or flame

Do Not Use

  • with electrocautery procedures
  • in the eyes
  • on mucus membrane
  • on irritated skin

Stop Use And Ask Doctor If

  • irritation or redness develops
  • if condition persists for more than 72 hours

Caution

In case of deep or punctured wounds, consult a doctor

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away

Directions For Use

  • wipe injection site vigorously and discard

Other Information

  • Store at room temperature 15-30⁰C (59-86⁰F)

Inactive Ingredient

purified water

Principal Display Panel

REF MW-APL

NDC 63517-500-02

alcohol prep pads

EN - Large 70% Isopropyl alcohol prep pad

FR - Tampon imbibe'd'alcool isopropylique a 70%, grand

ES - Almohadilla grande impregnada en alcohol isopropilico al 70%

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