Hand Sanitizer
FDA Label NDC 71734-328

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 Hand Sanitizer (NDC 71734-328). 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, keep out of reach of children., directions, inactive ingredients, product labeling, 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

  • Hand sanitizer to helo decrease virus on the skin when water,soap and towel are not available.
  • recommended for repeared use.

Warnings

For external use only. Avoid contact with the wound. Do not allow this product to come into contact with eyes or nearby.

If you accidently touch a wound or eye, rinse immediately with water.

If skin irritation or sensitivity occurs ,discontinue use and consult your doctor immediately.

Not recommended for infants.

Other information:

Store at 20℃（68 to 77 ℉）in a cool place . May discolor fabrics.

Keep Out Of Reach Of Children.

Do not allow children under 6 years of age to handle or apply this product，If swallowed ,contact your doctor immediately.

Directions

No water needed . Apply a small amount of product to dry skin.

Inactive Ingredients

Pure Water, Glycerine, Carbomer, Triethanolamine, Disodium EDTA

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