Royal Hand Sanitizer
FDA Label NDC 55439-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Gpm Investments Llc for the product Royal Hand Sanitizer (NDC 55439-000). 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

Ethyl Alcohol 62 percent

Purpose

Antimicrobial

Use

hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

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

When Using This Product

Do not use in eyes.
In case of contact with eyes, rinse with water

Stop Use And Ask A Doctor If

irritation and redness develops and persists.

Keep Out Of Reach Of Children

if swallowed, get medical help promptly.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Other Information

Store under 105 degrees F

Inactive Ingredients

Water, PEG12-Dimethicone, Carbomer, Fragrance. Aloe Barbadersis Leaf Juice, Triethanolamine.

Package Label

ROYAL ALOE Hand SanitizerCAUTION:EYE IRRITANT! MAY BE HARMFUL IF SWALLOWED.SEE CAUTION ON BACK PANEL.2 fl oz 60mlMade in China

* Please review the disclaimer below.