Alcohol Prep Swab
FDA Label NDC 70000-0112

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 (NDC 70000-0112). 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


  • To prepare skin prior to injection
  • To decrease germs in minor cuts and scrapes

Warnings

For external use only

Flammable. Keep away from fire or flame

Do Not Use

  • with electrocautery procedures
  • in the eyes
  • on mucous membranes
  • 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 puncture 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 59-86⁰F (15-30⁰C)
  • Avoid excessive heat

Inactive Ingredient

purified water

Principal Display Panel

NDC 70000-0112-1

LEADER

Alcohol Swabs

70% Isopropyl Alcohol

STERILE

Antiseptic for Preparation of Skin Prior to Injection

Latex Free

Extra Thick

Individually Wrapped Packets

COMPARE TO BD ALCOHOL SWABS

active ingredients*

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