Genius Care Hand Sanitizer 75 Percent Alcohol
FDA Label NDC 76114-008

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 Aidi Cosmetics Co., Ltd for the product Genius Care Hand Sanitizer 75 Percent Alcohol (NDC 76114-008). 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 other, active ingredient(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

NA

Active Ingredient(S)

Ethyl Alcohol 75% v/v

Purpose

Antispetic

Use

Hand sanitizer to help reduce bacteria that potentially can cause disease

For use when soap and water are not available

Warnings

For external use only

Flammable. Keep away from heat or flame

Do not use

  • on children less tha two months of age
  • on open skin wounds

Otc - When Using

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

Otc - Stop Use

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

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Place enough product on hands to cover all surfaces. Rub hands untill dry

Supervise children under six years of age when using this product to avoid swallowing

Other Information

Store between 15-30 C (59 to 86F)

Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

Water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, aloe barbadensis gel, carbomer, fragrance

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