First Aid Direct Alcohol Wipe Sponge
FDA Label NDC 42961-128

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cintas Corporation for the product First Aid Direct Alcohol Wipe (NDC 42961-128). 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 ingredient (in each towelette)

Isopropyl Alcohol 70%

Otc - Purpose

Purpose

Antiseptic cleanser 

Indications & Usage

Uses

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 and ask a doctor if irritation and redness develop

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 away. 

Dosage & Administration

Directions

wipe injection site vigorously and discard.

Other Safety Information

Other information

store at room temperature

Inactive Ingredient

Inactive ingredients

purified water

Otc - Questions

Questions? 

1-877-973-2811 M-F 8AM-5PM

Principal Display Panel

ALCOHOL WIPE

Saturated with 70% Isopropyl Alcohol 

For External Use Only 

Sterile unless package is damaged or opened

1 Wipe per Package

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