Acive Ingredient
ethyl Alcohol
Beverly Gel Hand Sanitizer Gel
FDA Label NDC 80586-801
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cleanslate Group Llc for the product Beverly Gel Hand Sanitizer (NDC 80586-801). 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 acive ingredient, inactive ingredients, dosage, indications, purpose, keep out of reach, warnings, 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
Inactive Ingredients
Water
Carbomer
Dimethicone PEG-8 Laurate
Glycerin
EDETOL
Fragrance
Aloe Barbadensis Leaf Juice
Dosage
Place enough product on your palm to thoroughly cover your hands
Rub hands together brisky until dry
Indications
Hand sanitizer to reduce microorganisms on skin
Use this product when soap and water are not available
Purpose
Antiseptic
Keep Out Of Reach
Keep out of reach of children. If swallowed get medical help or contact a Poison Control center right away
Warnings
For external use only. FLAMMABLE. This product contains ethyl alcohol. Keep away from flame
When using this product avoid contact with eyes.
Stop use and ask doctor if irritaiton or rash occurs.
* Please review the disclaimer below.
