Alcohol Prep Swab
FDA Label NDC 60913-018

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 (NDC 60913-018). 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 ingredients, purpose, use:, warnings:, keep out of reach of children., caution:, do not use, directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Isopropyl alcohol 70% v/v

Purpose

Antiseptic

Use:

For preparation of the skin prior to injection; to decrease germs in minor cuts and scrapes.

Warnings:

  • For external use only. Flammable; keep away from fire and flame.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center immediately.


Caution:

Do not apply to irritated skin.


Do Not Use

in the eyes, or on mucous membranes. In case of deep or puncture wounds, consult a doctor.


Directions:

Wipe injection site vigorously.


Other Information:

Store at room temperature


Inactive Ingredients:

Water

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Phoenix Healthcare Solutions,LLC

An Innovative Medical Manufacturer

NDC 60913-018-02

200 Individual Pads

Alcohol Prep Pads

Sterile - Medium

For Individual, Professional and Hospital Use

Saturated with 70% v/v Isopropyl Alcohol for external use only

Latex Free

Sterile in unopened, undamaged package

PIN DOT WOVEN

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