Alcohol Prep Pad Liquid
FDA Label NDC 59050-703
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Changzhou Maokang Medical Products Co., Ltd for the product Alcohol Prep Pad (NDC 59050-703). 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.
Do Not Use
- with electrocautery procedures
- in the eyes. If contact occurs, flush eyes with water.
Flammable, keep away from fire or flame.
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 Ingredients
purified water
Package Labelling;
Label.jpg (Label)
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