Otc - Active Ingredient
Ethyl Alcohol 62 %
Ben E.keith Gel
FDA Label NDC 50980-056
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ben E. Keith for the product Ben E.keith (NDC 50980-056). 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, warnings, otc - ask doctor, otc - when using, 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
Otc - Purpose
For handwashing 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.
Otc - When Using
To decrease bacteria on skin, apply a small amount to palm. Briskly rub, covering hands with product until dry.
Package Label.Principal Display Panel
Ben E. Keith Gel Sanitizer 8 oz. label
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