Esthete Hand Sanitizer
FDA Label NDC 55526-0014

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Eqmaxon Corp for the product Esthete Hand Sanitizer (NDC 55526-0014). 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, inactive ingredients, purpose, warnings, keep out of reach of children, uses, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 70.0%

Inactive Ingredients

PURIFIED WATER, ALOE EXTRACT, GLYCERIN, SODIUM HYALURONATE, CARBOMER, BUTYLENE GLYCOL, AMINOMETHYL PROPANOL, FRAGRANCE

Purpose

ANTISEPTIC

Warnings

▪ FOR EXTERNAL USE ONLY ▪ FLAMMABLE, KEEP AWAY FROM FIRE AND FLAME


When using this product
▪Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ▪ Avoid contact with broken skin ▪ Do not inhale or ingest.


Stop use and ask a doctor if irritation or redness develops.

Keep Out Of Reach Of Children

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

Uses

HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN

Directions

▪ DISPENSE ONE TO TWO PUMPS OF SANITIZER ONTO HANDS AND RUB THOROUGHLY UNTIL DRY.

▪ USE AS NEEDED ▪ FOR CHILDREN UNDER 6, USE WITH ADULT SUPERVISION

▪ NOT RECOMMENDED FOR INFANTS

Other Information

▪ Store below 110 °F(43°C)

▪ May discolor some fabrics

▪ Harmful to wood finishes and plastics

* Please review the disclaimer below.