Alcohol Prep Pad
FDA Label NDC 11673-600

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Alcohol Prep Pad (NDC 11673-600). 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, purpose, use, warnings, do not use, stop use, otc - ask doctor/pharmacist, otc - when using, 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

Purpose

Antiseptic

Use

For preparation of the skin prior to an injection

Warnings

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


Do Not Use

  • with electrocautery procedures
  • in the eyes

Stop Use

If irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Otc - Ask Doctor/Pharmacist


Otc - When Using


Otc - Pregnancy Or Breast Feeding


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.

Other


Other Information

Store at room temperature 15°- 30° C (59° - 86° F)

Inactive Ingredient

Purified water

Questions?

Call 1-800-910-6874

Package Information

Up and upNDC 11673-600-10alcohol prep pads70% isopropyl alcoholCompare to BD®*antiseptic for preparation of skin prior to injection100 count100 INDIVIDUALLY WRAPPED PADSDistributed by Target CorporationMinneapolis, MN 55403Made in U.S.A.© 2009 Target Brands, Inc.All Rights ReservedShop Target.com*This product is not manufactured or distributed by Becton Dickinson and Company, owner of the registered trademark BD®.

* Please review the disclaimer below.