Ultra Prep Alcohol Prep Pads Cloth
FDA Label NDC 83878-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Quality Medical Products Usa, Inc. for the product Ultra Prep Alcohol Prep Pads (NDC 83878-101). 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 drug facts, active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredient, 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 or redness develop. If your condition persists for more than 72 hours, consult a doctor.
Otc - Keep Out Of Reach Of Children
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 after single use.
Inactive Ingredient
purified water
Packaging
Ultrapreppad-101 (83878101 3)
* Please review the disclaimer below.
