Active Ingredient
Isopropyl Alcohol, 70% v/v
Alcohol Prep Pad
FDA Label NDC 72766-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yangzhou Suxiang Medical Instrument Co., Ltd. for the product Alcohol Prep Pad (NDC 72766-010). 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, uses, warnings, do not use, stop use and ask a doctor if, discontinue use and consult a healthcare practitioner if, 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
Purpose
Antiseptic, Sterile Solution
Uses
Antiseptic cleanser
Kills harmful bacteria and germs
First aid to help prevent infection
Warnings
For External Use Only
Avoid contact with the eyes
If contact occurs, flush eyes with water
Do Not Use
With electrocautery prodedures
In the eyes
Stop Use And Ask A Doctor If
Irritation and redness develops
If condition persists for more than 72 hours, consult a physician
Discontinue Use And Consult A Healthcare Practitioner If
Irritation develops
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
Use as part of your daily cleansing routine
May be covered with a sterile bandage
Other Information
Store at room temperature 15°-30°C (59°-86°F)
Avoid excessive heat
Inactive Ingredients
Water
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