Preference Hand Sanitizer
FDA Label NDC 62223-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Whip Mix Corporation for the product Preference Hand Sanitizer (NDC 62223-001). 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, use, warnings, otc - do not use, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient

→ Purpose

→ Use

→ Warnings

→ Otc - Do Not Use

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Inactive Ingredients

→ Principal Display Panel

Active Ingredient

Ethanol 72%

Purpose

Liquid Hand Sanitizer

Use

Used by Health Care Professionals for preventing the spread of both pathogenic microorganisms as well as resident bacterial flora and reducing healthcare-associated infections.

Warnings

Flammable, Keep away from fire or flame.

Otc - Do Not Use

For External Use Only

Do not get in the eyes. If splashed in eyes, rinse promptly and thoroughy with water. Discontinue use if irritation and redness develop. If irritation persists for more that 5 days, consult a physician.