Active Ingredient
Benzalkonium Chloride 0.2%
Antibacterial Wipes
FDA Label NDC 76635-009
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 Glamcos Biotech Co.,ltd for the product Antibacterial Wipes (NDC 76635-009). 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, otc - keep out of reach of children, directions, other safety information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Use
Hand sanitizer to help reduce bacteria on the skin.
Warnings
For external use only.
When using this product do not use in or near the eyes. In case of eye contact, rinse eyes with water.
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep out of reach of children .If swallowed,get medical help or contact a Posion control Center right away.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children .If swallowed,get medical help or contact a Posion control Center right away.
Directions
Wet hands thoroughly with product and allow to dry.
Dircard wipes in trash receptacle after use.Do not flush.
Children under 6 years of age should be supervised when using the product.
Other Safety Information
1.Fip open dispensing cap
2.Locate wipe at center of roll and thread tyrough small opening in lid
3.For best results dispense wipes at an angle
4.When finished snap lid cap shut to retain moisture
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Inactive Ingredients
Water………………………………….……….88.3000%
Propylene Glycol………………...……………1.0000%
DidecyldimoniumChloride……………………0.1000%
Phenoxyethanol…………………………........0.2000%
Chlorphenesin…………………………………0.1000%
Parfum(Fragrance)……………………………0.1000%
Alcohol……………… ………………………..10.0000%
Package Label
Label-70-1 (Label 70 1)
Label-70-2 (Label 70 2)
* Please review the disclaimer below.
