Hand Sanitizer Gel
FDA Label NDC 67777-911

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dynarex Corporation for the product Hand Sanitizer (NDC 67777-911). 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, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, 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

→ When Using This Product

→ Stop Use And Ask A Doctor If

→ Keep Out Of Reach Of Children.

→ Directions

→ Other Information

→ Inactive Ingredients

→ Label

Active Ingredient

Alcohol 70% V/V

Purpose

Antiseptic Handwash

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only

Flammable: Keep away from fire or flame

When Using This Product

• Do not get in the eyes

Stop Use And Ask A Doctor If

irritation and redness develop

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Wet hands thoroughly with product and allow to dry without wiping

Other Information

• Store at room temperature (15° - 30°C) (59° - 86°F)

• Recommended for repeated use

Inactive Ingredients

acrylates/C10-30 alkyl acrylate crosspolymer (60000 MPA.S), aloe barbadensis leaf juice, aminomethyl propanol, denatonium benzoate, fragrance, glycerin, propylene glycol, tocopheryl acetate, water