Clean Aid Antibacterial Hand Sanitizer
FDA Label NDC 71734-314

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Jiangmen Shuizirun Sanitary Articles Co., Ltd. for the product Clean Aid Antibacterial Hand Sanitizer (NDC 71734-314). 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, uses, warnings, consult a physicia, keep out of reach of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

  • decrease bacteria and germs on the hands
  • use when soap , towel and water are not available.
  • recommended for repeared use.

Warnings

For external use only.

Stop use and ask a doctor ifirritation or redness develops or persists.

Flammable, keep away from fire or flame

Do not apply around eyes.

Do not use in ears and mouth

Other information:

  • store at 20℃ (68 to 77 ℉)
  • may discolor fabrics

Consult A Physicia

if irritation or redness develops or persists

Keep Out Of Reach Of Children.

 Children under 6, use only under adult supervision. Not recommended for infants.

Directions

No water needed. Apply a small amount of product to dry skin. Rub briskly. wipe with paper towel or clean cloth or rinse with water and dry.

Inactive Ingredients

Aloe vera Gel, Extracts of juniper, Eucalyptus oil, Thymol, Essence (Radlx), Carbomer, Diisopropanol amine, Purified water

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