Active Ingredient
Isopropyl Alcohol 70%
Alcohol Prep Pad Liquid
FDA Label NDC 51142-444
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aso Llc for the product Alcohol Prep Pad (NDC 51142-444). 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 if, 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 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 If
irritation and redness develop. If condition continues, consult you health care practitioner.
Keep Out Of Reach Of Children
If swallowed get medical help or contact a Poison Control Center right away.
Directions
wipe ingection area and discard
Other Information
Store at room temperature: 59°F - 86°F (15°C - 30°C)
Inactice Ingredient
purified water
Principal Display Panel
ALCOHOL PREP PAD
1 Pad/Pouch
Saturated with 70% Isopropyl Alcohol
For External Use Only
DO NOT REUSE
NOT MADE WITH NATURAL RUBBER LATEX
* Please review the disclaimer below.
