Otc - Active Ingredient
Ethanol
Hand Sanitizing Wipes Patch
FDA Label NDC 84449-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Benliju Bio-tech Co.,ltd for the product Hand Sanitizing Wipes (NDC 84449-007). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Hand sanitizer to help reduce bacteria on the skin
Indications & Usage
Hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable,Keep away from fire or flame
Otc - Do Not Use
When using this product do not use in ornear the eyes.In case of contact, rinse eyes thoroughly with water.
Otc - When Using
When using this product keep out of eyes.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children,lf swallowed, get medical help contact POISON CONTROL CENTER right away.
Dosage & Administration
Directions: Tear open, unfold and apply to hands, discard after usee Children should be supervised when using this product.
Storage And Handling
Store at room temperature.
Inactive Ingredient
Aqua (Water), Aloe Barbadensis Leaf Extract, Glycerin, Tocopheryl Acetate, Fragrance (Aloe Vera Scent).
Package Label.Principal Display Panel
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Package (Package(1))
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