Asepso Hand Sanitizer
FDA Label NDC 73931-014

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Essence Daily Chemical Co., Ltd for the product Asepso Hand Sanitizer (NDC 73931-014). 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, keep out of reach of children., directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 72% v/v

Purpose

 Antiseptic

Use

  • A hand sanitizer to decrease bacteria on the skin.
  • Recomended for repeated use.

Warnings

For external use only.

Flammable,

Keep product away from heat or flame.

When using this product

do not use in the eyes, In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or redness develop and persist for more than 72 hours.

Keep Out Of Reach Of Children.

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

Directions

  • Wet hands thoroughly with product.
  • Briskly rub hands together until dry
  • Supervise children under 6 years in the use of this product.

Inactive Ingredients

Water, Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice.

* Please review the disclaimer below.