Alcohol Prep Pad Swab
FDA Label NDC 34645-3111

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Jianerkang Medical Co., Ltd for the product Alcohol Prep Pad (NDC 34645-3111). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredients

Isopropyl Alcohol 70%

Otc - Purpose

Purpose

Antiseptic

Indications & Usage

Use

For preparation of the skin prior to an 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, if contact occurs, flush eyes with water

Otc - Stop Use

Stop Use

If irritation and redness develop.

If condition persists consult your health care practitioner

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

If swallowed, get medical help or contact Poison Control Center right away

Dosage & Administration

Directions

Wipe injection site vigorously and discard

Storage And Handling

Other Information

Store at room temperature 15 o-30 o C (59 o-86 o F)

Inactive Ingredient

Inactive Ingredient

purified water

Package Label

Pouch Label (Pouch)

Pouch Label (Pouch)

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