Toprosan Hand Sanitizer
FDA Label NDC 80149-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Toprosan-valuerays for the product Toprosan Hand Sanitizer (NDC 80149-001). 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, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol 75% v/v.

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. Use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do Not Use

on children under 2 months old

or on open skin wounds.

When using this product keep out of eyes, ears, mouth. In case of eye contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

Place enough sanitizer on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years old when using this product to avoid swallowing.

Inactive Ingredients

Hydrogen peroxide, USP purified water.

* Please review the disclaimer below.