Babyliss Pro Protect Hand Sanitizer
FDA Label NDC 78080-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Makmac Inc for the product Babyliss Pro Protect Hand Sanitizer (NDC 78080-002). 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, use, warnings, when using this product, stop use and ask doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl Alcohol 70% V/V

Purpose

Antiseptic

Use

Antibacterial hand sanitizing gel to help kill bacteria and germs as antiseptic on the skin. For use when soap and water are not available.

Warnings

Flammable. Keep away from fire or flame.

For external use only

When Using This Product

keep out of eyes and mouth. In case of contact with eyes, immediately rinse eyes thoroughly with water.

Stop Use And Ask Doctor If

irritation, rash or allergy occurs. These may be signs of a serious condition.

Keep Out Of Reach Of Children.

If swallowed get medical help or contact a poison control center right away.

Directions

Apply. Put enough product on hands to cover all surfaces. Rub hands together, until hands feel dry. This should take around 20 seconds. Recommended for repeated use. Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

Store between 59-86°F (15-30°C)
Avoid freezing and excessive heat above 104°F (40°C)

Inactive Ingredients

Deionized Water. Carbomer. Panthenol. DMDM Hydantoin. Disodium EDTA. Triethanolamine.

Package Labeling

Bottle (Bottle)

Bottle (Bottle)

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