Youmi Alcohol Prep Pad 70 Isopropyl Alcohol Liquid
FDA Label NDC 87401-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pt Youmi Medika Industri for the product Youmi Alcohol Prep Pad 70 Isopropyl Alcohol (NDC 87401-000). 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 and ask a doctor 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%
Purpose
Antiseptic Cleanser
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. If contact occurs, flush eyes with water.
Stop Use And Ask A Doctor If
irritation and redness develop.
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 Information:
Store at room temperature.
Inactive Ingredient:
Purified Water.
Package Labeling:
Label (Label)
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