Active Ingredient
70% Ethyl Alcohol
Hand Sanitizer
FDA Label NDC 71734-302
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 71734-302). 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, warnings, keep out of reach of children., directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand sanitizer to help decrease virus on the skin.
When water, soap and towel are not available
Recommended for repeated use.
Warnings
For external use only.
For external use only.
Avoid contact with the wound.
Do not allow this product to come or nearby.
If you accidentally touch a wound or eye, rinse immediately with water.
If skin irritation or sensitivity occurs, discontinue use immediately and consult your doctor imediately.
Not recommended for infants.
Keep Out Of Reach Of Children.
Do not allow children under 6 years of age to handle or apply this product.
If swallowed carelessly, contact your doctor immediately.
Directions
Pump as needed into your palms and thoroughly spread on both hands.
Rub into skin until dry.
Inactive Ingredients
Pure Water, Glycerin, Carbomer, Triethanolamine, Disodium EDTA
* Please review the disclaimer below.
