Colorrose Hand Sanitizer
FDA Label NDC 78163-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Cheerflor Cosmetics Co., Ltd. for the product Colorrose Hand Sanitizer (NDC 78163-001). 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 drug facts, [active ingredient], [purpose], [inactive ingredients], [use], [directions], [warnings], 3.when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

[Active Ingredient]

Alcohol 75% v/v

[Purpose]

Sterilization

[Inactive Ingredients]

Aqua, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Triethanolamine, Glycerin, Propylene Glycol, Aloe Vera Extract.

[Use]

Hand disinfection. Helps reduce bacteria on the skin and kills most common germs that may cause illness.

[Directions]

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

[Warnings]

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

3.When Using This Product

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

Stop Use And Ask A Doctor

if irritation on rash appears and lasts.

4.Keep Out Of Reach Of Children.

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

Package And Labeling 30Ml

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Package And Labeling 50Ml

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Package And Labeling 1000Ml

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