Active Ingredient
Benzalkonium chloride 0.08%
Alcohol Free Hand Sanitizing Wipes
FDA Label NDC 71766-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hangzhou Linkeweier Daily Chemicals Co. Ltd. for the product Alcohol Free Hand Sanitizing Wipes (NDC 71766-006). 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, warning, when using this product, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
- For handwashing to decrease bacteria on the skin.
- After changing diapers.
- After assisting ill persons.
- Before contact with a person under medical care or treatment.
- Recommended for repeat use.
Warning
For external use only.
Do not use in the eyes.
When Using This Product
When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.
Stop Use And Ask A Doctor If
Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
Keep Out Of Reach Of Children
Keep out of reach from children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Wet hands thoroughly with product and allow to dry.
- Children under six years of age should be supervised when using this product.
Other Information
Store in a cool, dry place.
Inactive Ingredient
Decyl Glucoside，Polyaminopropyl Biguanide，Phenoxyethanol， Didecyl Dimethyl Ammonium Chloride，Aloe Barbadensis Leaf Juice Glyceri，Vitamin E, Water
Package Label
800 IN A BAG NDC: 71766-006-01
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