Active Ingredient
Isopropyl Alcohol, 70% v/v
Ultra-care Alcohol Prep Pad
FDA Label NDC 72217-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Arise Medical Llc for the product Ultra-care Alcohol Prep Pad (NDC 72217-001). 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, use, warnings, do not use, consult a doctor, caution, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For preparation of the skin prior to injection
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do Not Use
in the eyes or on mucous membrane
Consult A Doctor
In case of deep or punctured wounds
Caution
Do not apply to irritated skin
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
wipe injection site vigorously
Inactive Ingredient
Water
Other Information
Store at room temperature
Principal Display Panel
NDC: 72217-001-01
Ultra-Care Alcohol Prep Pads
MEDIUM 2-PLY PREP PAD
STERILIZED WITH GAMMA RADIATION
Latex FREE
100
Label 1 (01)
NDC: 72217-001-02
Ultra-Care Alcohol Prep Pads
MEDIUM 2-PLY PREP PAD
STERILIZED WITH GAMMA RADIATION
Latex FREE
200
Label 2 (02)
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