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Drug Facts
Prosilk Hand Sanitizer
FDA Label NDC 78242-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Diamo Kozmetik Sanayi Ic Ve Dis Ticaret Limited Sirketi for the product Prosilk Hand Sanitizer (NDC 78242-001). 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 other, active ingredient, purpose, use, warnings, uses, 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
Active Ingredient
Ethyl Alcohol, 70%..................
Purpose
Antiseptic
Use
Flammable . keep away from sources of ignition-no smoking.
Warnings
for external use only.
Uses
In cases of contact with eyes, wash immediately.
Do not innhale or ingest.
Avoid contct with beoken skin.
Keep Out Of Reach Of Children
In cases of accidental ingestion,seek medical advice immediately.
Keepaway from food sources.
Directions
Wet hands thoroughly with product and rub until dry without wiping.
Use without water.
Inactive Ingredients
Alcohol,Aqua,Glycerin,trinethanolamine,Acrylates/C10-30 Alkyl Acrylare Crosspolymer, Parfum, Aloe Barbadensis Leaf Juice,HexylCinnamal,
Geraniol,Butypheny methlypropinal, Linalool, Limonene.
Please see label on the container.
Package Label.Principal Display Panel
Alo (Alo)
Proslik250 (Proslik250)
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