Ethyl Alcohol Wet Wipes
FDA Label NDC 73796-003

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Prostock Llc for the product Ethyl Alcohol Wet Wipes (NDC 73796-003). 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 drug facts, active ingredient, purpose, uses, warnings, do not use, stop use & ask doctor, keep out of reach from children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl Alcohol (70.00% V/V)

Purpose

Antiseptic

Uses

  • For hand-washing to decrease bacteria on skin

Warnings

Flammable. Keep away from heat and flame.
For External use only.

Do Not Use

in eyes. In case of contact, rinse thoroughly with water.

Stop Use & Ask Doctor

if rash/redness or irritation appears/develops and persist for more than 72 hours.

Keep Out Of Reach From Children

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

Directions

  • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation. 
  • Thoroughly wipe hands, allow to dry without washing.
  • Discard after single use

Other Information

  • Do not flush down toilet. 
  • Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit) 
  • May discolor certain fabrics

Inactive Ingredients

Aqua, Glycerin, Aloe Barbadensis Leaf Juice, D-Panthenol, Phenoxyethanol

Package Labeling:15Pcs

Bottle (Bottle)

Bottle (Bottle)

Package Labeling:50Pcs

Bottle2 (Bottle2)

Bottle2 (Bottle2)

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