Devobis Hand Sanitizer
FDA Label NDC 90030-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Erte Kozmetik Sanayi Ve Ticaret Anonim Sirketi for the product Devobis Hand Sanitizer (NDC 90030-001). 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 drug facts, active ingredient, purpose, use:, warnings:, do not use, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 80%(v/v)
Purpose
Antiseptic
Use:
- Hand sanitizer to help decrease bacteria on the skin
- Recommended for repeat use
Warnings:
For external use only
Flammable, keep away from fire and flames
Do Not Use
in the eyes, In case of contact, rinse eyes thoroughly with water
Stop Use And Ask A Doctor If
- Irritation and redness develop
- Condition persist for more than 72 hours
Keep Out Of Reach Of Children
If swallowed, seek medical attention immediately or contact a Poison Contrl Center. Children must only use this product under adult supervision.
Directions:
Place small amount of sanitizer in your palm. Thoroughly spread on both hands and rub together until dry.
Other Information:
Store below 110 °F
Inactive Ingredients:
Aqua (Water), Glycerin, Acrylates/C 10-30 Alkyl Acrylate Crosspolymer, Hydrogen Peroxide, Aminomethyl Propanol.
Package Labeling:
Box (Box)
* Please review the disclaimer below.
