Antiseptic Disinfectant
FDA Label NDC 77217-200

The antiseptic disinfectant is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

Ethyl Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (96%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Ethyl Alcohol 96% v/v. Purpose: Antiseptic

Antiseptic

Antiseptic Disinfectant to help reduce bacteria that potentially can cause disease.

For external use only. Flammable. Keep away from heat or flame

in children less than 2 months of age

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Place enough product to clean the infected area
Supervise children under 6 years of age when using this product to avoid swallowing.

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

purified water USP

1000 mL NDC: 77217-200-05