Otc - Active Ingredient
Sodium Chloride
Bye Zero
FDA Label NDC 80762-0021
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Korea Life Science for the product Bye Zero (NDC 80762-0021). 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, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, 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
Inactive Ingredient
Kelp extract, Seaweed extract, magnesium extract, calcium extract, potassium extract, sulfate ion extract, water
Otc - Purpose
Hand sanitizer to help reduce bacteria that potentially can cause disease. for use when soap and water are not available.
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
place enough product on hadns to cover all surfaces. rub hands together until dry.
supervise children uner 6 years of age when using this product to avoid swallowing.
Warnings
Stop use and ask a doctor if irritation or rash occurs.
Keep out of reach of children.
Dosage & Administration
for external use only
Package Label.Principal Display Panel
Label (Label)
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