Drug Facts Active Ingredient
Ethyl Alcohol 62.0%
Advanced Hand Sanitizer
FDA Label NDC 72308-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Flex Beauty Labs, Llc for the product Advanced Hand Sanitizer (NDC 72308-001). 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, uses, warnings, when using this product,, directions:, other information:, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
Hand Santizer to help reduce bacteria on skin that may cause disease.
Warnings
Flammable. Keep away from heat or flame.
For external use only.
When Using This Product,
do not use in or near the eyes. In case of contact, rinse eyes thoroughtly with water. Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach for children.
If swallowed, get medical help or contact a Posion Control Center right away.
Directions:
. Place enough Product in your palm to thoroughtly spread on both hands and rub into the skin until dry.
. Children under 6 years of age should be supervised when using this product.
Other Information:
. Store below 106℉. (41℃)
Inactive Ingredients:
Water (Aqua), Aloe Vera Leaf , Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine,
* Please review the disclaimer below.
