Otc - Active Ingredient
Benzalkonium Chloride 0.13%
Hand Sanitizer Gel
FDA Label NDC 81726-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Source Design Collections for the product Hand Sanitizer Gel (NDC 81726-002). 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, uses, inactive ingredient, directions, warnings, otc - do not use, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Uses
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Inactive Ingredient
Water(aqua), propylene glycol, hydroxyethylcellulose, phenoxyethanol, alcohol
Directions
Place enough product on hands to cover all surfaces.Rub hands together until dry.
Warnings
For external use only.
Otc - Do Not Use
Do not use on open skin wounds or children under 2 months of age.
Otc - When Using
When using this product keep out of eyes,ears, and mouth. ln case of contact with eyes,rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs.These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.
Other Information
Store in a cool dry place, away from direct sunlight and heat.
Package Label.Principal Display Panel
Label (Label)
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