Alcohol Pad Solution
FDA Label NDC 72459-014
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yiwu Ori-power Medtech Co.,ltd. for the product Alcohol Pad (NDC 72459-014). 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 ingredients, purpose, inactive ingredients, use, directions, storage, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Isopropyl Alcohol 70%v/v.
Purpose
First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.
Inactive Ingredients
Purified Water.
Use
Cleaning and preparing skin for medical procedures.
Directions
Tear open packet, use alcohol pad to cleanse desired skin area or surfaces. Discard pad appropriately after use.
Storage
Store at room temperature 15°C-30°C (59°F-56°F).
Warnings
Flammable, keep away from fire or flame. Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If irritation develops for more than 72 hours, consult physician.
Do Not Use
with electocautery procedures.
Keep Out Of Reach Of Children
In case of accidental swallowing, seek medical help and contact poison control immediately.
Package Labeling:
Label (Label)
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