Joylux Anti Bacterial Hand Sanitizer
FDA Label NDC 71734-301

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 Joylux Anti Bacterial Hand Sanitizer (NDC 71734-301). 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, when using this product, keep out of reach of children., dosage & administration, 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

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.

Avoid contact with the wound. 

Do not allow this produts to come into contact with eyes 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.

Not recommended for infants. 

When Using This Product

Dn not allow children under 6 years of age to handle or apply, contact your doctor immediately.

Keep Out Of Reach Of Children.

If swalllowed carelessly, contact your doctor immdiately.

Dosage & Administration

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

Inactive Ingredients

Triethanolamine, Carbomer, Glycerine, Disodium EDTA, Pure Water

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