Active Ingredients
E0.13% Benzylkonium Chloride
Peter Pan
FDA Label NDC 52305-400
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Freshorize, Ltd. for the product Peter Pan (NDC 52305-400). 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 ingredients, indications & usage, warnings, otc - keep out of reach of children, otc - purpose, dosage & administration, inactive ingredient, 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
Indications & Usage
Requires no water or towels. Apply small amount to hands and rub lightly until dry.
Warnings
Safety: Avoid contact with Eyes, should this occur rinse immediately with clean warm water.
Caution: Use on hands only.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Purpose
Kills 99.9% Bacteria
Dosage & Administration
Requires no water or towels.
Apply small amount to hands and rub lightly until dry.
Inactive Ingredient
Aqua, Polysorbate 40, Aloe Barbadensis, Parfum
Package Label.Principal Display Panel
Peter Pan Label (Peterpan Alc Free Label)
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