Otc - Active Ingredient
Isopropyl Alcohol, 70% by volume
Alcohol Prep Pads Swab
FDA Label NDC 60913-207
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Phoenix Healthcare Solutions Llc for the product Alcohol Prep Pads (NDC 60913-207). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Indications & Usage
For preparation of the skin prior to injection
Warnings
For external use only. Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use with electrocautery procedures, or in/near eyes.
Otc - Stop Use
Stop use if irritation or redness develops. If irritating condition persists for more than 72 hours, consult a physician.
Otc - Keep Out Of Reach Of Children
If swallowed, seek medical attention and/or contact a Poison Control Center immediately.
Dosage & Administration
Prepare site by wiping vigorously.
Storage And Handling
Store at 4-35C. Avoid direct sunlight.
Inactive Ingredient
Purified water
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