This is a hand sanitizer manufactured according to the 1994 tentative final monograph for consumer antiseptics.
The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation):
- Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (75%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
- hydroxyethylcellulose
- aloe powder
- propylene glycol
- hyaluronic acid
- tea tree essential oil
- vitamin E
- Sterile distilled water or boiled cold water.
The firm does not add other active or inactive ingredients. The product has undergone finished formulation product testing (kill study) to confirm effifacy and safety.