Active Ingredient
Active Ingredient (Label)
Hand Sanitizer
FDA Label NDC 78837-202
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Phoenix Wipes Inc for the product Hand Sanitizer (NDC 78837-202). 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, dosage & administration, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, warnings, 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
Dosage & Administration
Active Ingredient (Label)
Inactive Ingredient
Active Ingredient (Label)
Indications & Usage
Active Ingredient (Label)
Otc - Keep Out Of Reach Of Children
Active Ingredient (Label)
Otc - Purpose
Active Ingredient (Label)
Warnings
Active Ingredient (Label)
Package Label.Principal Display Panel
2ml NDC 78837-202-20
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