Active Ingredient
Benzalkonium Chloride 0.13%
Ubamong Disinfecting Wipes
FDA Label NDC 80002-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shaoxing Ailan Non-woven Fabric Products Co., Ltd. for the product Ubamong Disinfecting Wipes (NDC 80002-001). 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, warning, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For Hand Sanitizing
Warning
■For external use only
■Flammable. Keep away from fire or flame
When using this product
■Do not use in or near the eyes. In case of contact
with eyes flush thoroughly with water
■Use wipes only on unbroken, intact skin
■If you have sensitive skin or certain allergies,
check the list of ingredients on the label before using wipes
■Do not ingest
Stop use and ask a doctor
■If skin irritation or redness develops
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
■Children under 6 years of age use only under adult supervision
Directions
■Wipe hands thoroughly, let skin dry and discard
■Not recommended for infants
Inactive Ingredients
Aqua, Propylene Glycol, Phenoxyethanol.
Package Label.Principal Display Panel
1 (80002001)
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