Bolisi Dispsable Hand Sanitizer
FDA Label NDC 75255-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Baoli Cosmetics Co., Ltd. for the product Bolisi Dispsable Hand Sanitizer (NDC 75255-002). 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, otc - keep out of reach of children, warnings:, dosage & administration, 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 75%±5% (V/V)

Purpose

 Antiseptic

Use

hand sanitizer to help decrease bacteria on the skin and recommended for repeated use.

Otc - Keep Out Of Reach Of Children

Children must be supervised in use of this product.

Warnings:

  • For external use only.
  • Flammable.
  • Keep away from fire or flame.
  • Do not apply around eyes.
  • Do not use in ears and mouth.

    • When using this product, Avoid contact with eyes. In case of contact flush eyes with water.

    Stop use and ask a doctor if irritation or rash appears on the skin.

Dosage & Administration

Place enough product in your palm to thoroughly cover your hands rub together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Other Information: 

  • Do not store above 85℉.
  • May discolor certain fabrics or surfaces.

Inactive Ingredients

Water, Proplene Glycol, Triethanolamine, Carbomer.

* Please review the disclaimer below.