Active Ingredient Purpose
Benzalkonium Chloride 0.13%...Antimicrobial
All Day Hand Sanitizer
FDA Label NDC 79039-300
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bpi Packaging, Llc for the product All Day Hand Sanitizer (NDC 79039-300). 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, otc - purpose, dosage and administration, warnings, otc - when using, otc - stop use, otc - 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
Otc - Purpose
Antimicrobial
Dosage And Administration
Directioins: Apply liberally to the hands and gently rub ubtil dry
Warnings
For External use Only.
Otc - When Using
When Using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Pioson Control Center immediately.
Directions
Apply liberally to the hands and gently rub until dry.
Other Information
Store at room temperature
Inactive Ingredients
1-Octadecanaminium N, N Dimethyl-N-(3(Trihydroxysilyl) Propyl) Chloride, Water
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