Alcohol Prep Pad
FDA Label NDC 34645-3031

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Jiangsu Province Jianerkang Medical Dressing Co. ,ltd. for the product Alcohol Prep Pad (NDC 34645-3031). 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 package label.principal display panel, otc - active ingredient, otc - purpose, otc - when using, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Package Label.Principal Display Panel

Cat. 40000-110    NDC 34645-3031-5    Qty.1eaAlcohol Prep PadAntiseptic *Sterile, Medium, 2-ply * Saturated with 70% isopropyl alcohol * Sterile if unopened, undamaged * For External Use OnlyDistributed by:Cardinal HealthDublin, OH 43017 USAMade in China
Image of Pouch Label

Otc - Active Ingredient

Active ingredient
Isopropyl Alcohol, 70% v/v

Otc - Purpose

Purpose
Antiseptic

Otc - When Using

Use
For preparation of skin prior to injection

Warnings

Warnings
For external use only.
Flammable, keep away from fire or flame.

Otc - Do Not Use

Do not use
with electrocautery procedures, in the eyes.

Otc - Stop Use

Stop use
if irritation or redness develop. If the condition persists for more than 72 hours, consult a doctor.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right way.

Indications & Usage

Directions
Wipe injection site vigorously and discard

Inactive Ingredient

Inactive ingredient
purified water

* Please review the disclaimer below.