Fresh Up Antiseptic Hand
FDA Label NDC 53859-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by G&g Medical Products Llc for the product Fresh Up Antiseptic Hand (NDC 53859-001). 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, keep out of reach of children., directions, other information, 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

→ Uses

→ Warnings

→ Keep Out Of Reach Of Children.

→ Directions

→ Other Information

→ Inactive Ingredients

→ Package Labeling

Active Ingredient

Ethyl Alcohol 70 percent

Purpose

Antiseptic

Uses

For hand washing to decrease bacteria on the skin.

Warnings

Flammable, keep away from fire or flame

For external use only.

Do not use

in the eyes
In case of eye contact, flush eyes with water.

Stop use and ask a doctor

Keep Out Of Reach Of Children.

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

Directions

Spray enough product to thoroughly cover and wet hands. Rub hands together until dry. Children under 6 years of age should be supervised when using product.