Active Ingredient
Isopropyl Alcohol, 70% v/v
Alcohol Prep Pad Medium Cloth
FDA Label NDC 87993-101
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 Huanrui Medical Technology Co., Ltd for the product Alcohol Prep Pad Medium (NDC 87993-101). 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, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For preparation of skin prior to injection
Warnings
Flammable - keep away from fire or flame.
For external use only.
Do Not Use
- with electrocautery procedures
- In the eyes
Stop Use
If Irritation or redness develops.
If the condition persists for more than 72 hours, consult a doctor.
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
Inactive Ingredients
purified water
Package Label.Principal Display Panel
Alcohol Prep Pad Label (Sx1049)
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