Kentex Alcohol Prep Pad Saturated With Isopropyl Alcohol Liquid
FDA Label NDC 69556-804
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kentron Healthcare, Inc. for the product Kentex Alcohol Prep Pad Saturated With Isopropyl Alcohol (NDC 69556-804). 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 drug facts, active ingredient, purpose, use, warnings, do not use, stop use 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
Active Ingredient
Isopropyl Alcohol,70% v/v
Purpose
Antiseptic
Use
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.
Stop Use If
irritation of redness develop. If the condition persists for more than 72 hours, consuIt a doctor,
Keep Out Of Reach Of Children.
lf swallowed, get medical help or contact a Poison Control Center right away.
Directions
wipe injection site vigorously and discard
Inactive Ingredient
purified water
Package Labeling:
Label (Label)
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