Asepso Sani Care Alcohol Sanitizer
FDA Label NDC 73931-010

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 Sani Care Alcohol Sanitizer (NDC 73931-010). 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

Alcohol 75% v/v

Purpose

 Antiseptic

Use

Sanitizing disinfectant to help reduce bacteria that potentially can cause disease. For use when soap ad water are not avilable.

Warnings

For external use only.

Flammable,

Keep away from heat and flame.

Do not use

  • On children less than 2 months of age 
  • On broken skin.

    • When using this product keep out of eyes, ears, and mouth. In case of contact, rinse thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep Out Of Reach Of Children.

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

Directions

  • For best results apply a generous amount to a clean cloth and thoroughly clean areas that need to be disinfectant.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive Ingredients

Water USP, Denatonium Benzoate.

* Please review the disclaimer below.