Otc - Active Ingredient
Benzethonium chloride 0.2 %
Ben E. Keith
FDA Label NDC 50980-682
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 Foods for the product Ben E. Keith (NDC 50980-682). 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, otc - keep out of reach of children, indications & usage, warnings, 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
Otc - Purpose
Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a poison control center.
Indications & Usage
To decrease bacteria on skin, apply small amount of product to palms. Briskly rub, covering hands with product until dry.
Warnings
For external use only. Avoid contact with eyes. If contact occurs, flush with water.
Dosage & Administration
To decrease bacteria on skin, apply small amount to palm. Briskly rub, covering hands with product until dry. Children should be supervised when using product.
Inactive Ingredient
Water, Fragrance, Aloe Barbadensis, Tocopheryl Acetate, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Propylene Glycol, Phenoxyethanol, Tetrasodium EDTA
Package Label.Principal Display Panel
Foaming Instant Hand Sanitizer Bag Label
Ben E. Keith Foaming Ihs Label (Benekeithfmihs 1000mlbag)
* Please review the disclaimer below.
