Freshnap Plus - 80% Ethyl Alcohol Towelette Cloth
FDA Label NDC 79985-200

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Kari-out Llc for the product Freshnap Plus - 80% Ethyl Alcohol Towelette (NDC 79985-200). 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, stop using and ask a doctor if, keep out of reach of children, do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl Alcohol 80% (v/v)

Purpose

Antiseptic

Uses

  • hand sanitizer to help reduce bacteria on the skin.

Warnings

  • Flammable. Keep away from heat or flame.
  • For external use only. Avoid contact with eyes, ears and mouth. In case of eye contact, flush with water.

Stop Using And Ask A Doctor If

  • skin irritation or redness develops.

Keep Out Of Reach Of Children

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

Directions

  • Unfold towelette, wipe hands thoroughly and discard.

Inactive Ingredients

Denatonium Benzoate, Glycerin, Hydrogen Peroxide, Aqua (Water)

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