Otc - Active Ingredient
Ethyl Alcohol 62 % v/v
Alcoscrub
FDA Label NDC 55863-700
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Erie Scientific, Llc. for the product Alcoscrub (NDC 55863-700). 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, otc - purpose, keep out of reach of children, indications & usage section, warnings, otc - ask doctor, dosage & administration section, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
For handwashing to decrease bacteria on skin.
Keep Out Of Reach Of Children
If swallowed, contact a physician or poison center
Indications & Usage Section
For hand cleaning to decrease bacteria on skin
Warnings
Flammable. Keep away from heat of flames. For external use only. Do not use in the eyes.
Otc - Ask Doctor
Discontinue use if redness and irritation develop. If condition persists for more than 72 hours, consult a physician. If swallowed, contact a physician or poison control center. Keep out of the reach of children.
Dosage & Administration Section
Apply a small amount to palm. Briskly rub, covering hands with product until dry.
Inactive Ingredients
Water, Glycerin, Carbomer, Propylene glycol, Isopropyl Myristate, Triethanolamine, Aloe Barbadensis Leaf, Tocopheryl acetate
Package Label.Principal Display Panel
Alcoscrub800ml (Alcoscrub800ml)
* Please review the disclaimer below.
