Active Ingredient
Isopropyl alcohol 70% v/v
Cut Care Alcohol Prep Pad
FDA Label NDC 53439-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zeus Medical Holdings Llc for the product Cut Care Alcohol Prep Pad (NDC 53439-100). 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, stop use and ask a doctor 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
Purpose
Antiseptic
Use
For preparation of the skin prior to injection
Warnings
- For external use only
- Flammable, keep away from flame or fire
- Not for use with electrocautinary devices or procedures
- Do not use in eyes
- Sterile unless package is damaged or open.
Stop Use And Ask A Doctor If:
- Irritation or redness develops
- condition persists for more than 72 hours
Keep Out Of Reach Of Children.
In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.
Directions
- Wipe injection site vigorously and discard
Other Information
store at room temperature: 15○ - 30○C (59○F – 86○F)
- avoid excessive heart
Inactive Ingredient
purified water
Principal Display Panel
NDC 53439-100-10
Cut Care
Alcohol Prep Pad
Saturated with 70% Isopropyl Alcohol
Contents: 100 Pouches
Principal Display Panelndc 53439-100-10cut Carealcohol Prep Padsaturated With 70% Isopropyl Alcoholcontents: 100 Pouches (Cut Care Alcohol Prep Pad 01)
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