Active Ingredient
Ethanol 70%
Dr.better Homes Hand Sanitizer
FDA Label NDC 75615-0020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ui Cosmetics Co., Ltd for the product Dr.better Homes Hand Sanitizer (NDC 75615-0020). 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 active ingredient, purpose, uses, warnings, when using this product, stop use and ask doctor if, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
To help reduce bacteria on the skin
Warnings
For external use only.
Flammable, keep away from heat or flames.
When Using This Product
keep away from eyes. In case of eye contact, rinse eyes with water.
Stop Use And Ask Doctor If
irritation and redness develop and persist.
Directions
Apply a small amount in your palm and rub hands together briskly until dry.
Supervise children under 6 years in the use of product.
Other Information
Protect this product from excessive heat and direct sun.
Inactive Ingredient
Glycerin, Sodium Hyaluronate, Carbomer, Butylene Glycol, Aloe Extract, Triethanolamine, Flavoring, Purified Water
* Please review the disclaimer below.
