Viloe
FDA Label NDC 78733-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sonora Corporation for the product Viloe (NDC 78733-001). 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 active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 75% v/v.

Purpose

Antiseptic

Uses

For sanitizing to help reduce bacteria on the skin.

Warnings

For external use only. Flammable. DO NOT store above 1050F. Keep away from heat or flame.

Do not use

  • in or near the eyes.
  • on open skin wounds or burns.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children, unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Open lid, gently pull back resealable label, remove and use wipe as required.
  • Reseal back after use to avoid evaporation of alcohol.

    • Other information
    This product is insoluble in water. Dispose of used wipe in trash, do not flush into toilet. This product may discolor certain fabrics or surfaces.

Inactive Ingredients

Water (Aqua)

Package Label - Principal Display Panel

Label (Label)

Label (Label)

* Please review the disclaimer below.