Active Ingredient (In Each Towelette) ............Purpose
Isopropyl Alcohol 70%..........Antiseptic
Alcohol Pad
FDA Label NDC 71105-111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Redicare Llc for the product Alcohol Pad (NDC 71105-111). 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 (in each towelette) ............purpose, use:, warnings:, do not use:, stop use if, keep out of reach of children., directions:, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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 and redness develop. If condition persists consult your health care practitioner.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison COntrol Center right away.
Directions:
Wipe injection area and discard.
Other Information:
Store at room temperature 15 o to 30 oC (59 o to 86 oF).
Inactive Ingredient:
water
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