Active Ingredient
Ethyl Alcohol 71%
The following Structured Product Label (SPL) was submitted to the FDA by Skaffles Group Limited Liability Company for the product Hand Sanitizer (NDC 77720-018). 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, use, warning, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Ethyl Alcohol 71%
Antiseptic
Hand sanitizing to help reduce bacteria on the skin. Recommended for repeated use.
For external use only./ Para uso externo uinicamente.
Do not use / No utilice o lf you are allergic to any of the ingredients. o In the eyes;if contact occurs, rinse thoroughly with water.i Si es alergico a alguno de losingredientes.ยท Si entra en contacto con los ojos,enjuague por completo con agua.Discontinue use ifiritation and redness develop. lf condition persists for morethan 72 hours consult a doctor./Suspenda el uso si se presenta irritacion yenrojecimiento.Consulte a un medico si la condicion persiste por mas de 72 horas.Keep out of reach of children. If swallowed, get medical help or contact aPoison Control Center right away./ Mantengase fuera del alcance de los niios.Sise ingiere, obtenga atencion medica o pongase en contacto de inmediato conun Centro de control de envenenamientos.
Keep out of reach of children. If swallowed, get medical
help or contact a Poison Control Center right away.
Adtults and children 2 yrs and over, apply to hands and allow skin to dry without wiping. Children under 2, ask doctor before use.
Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Propylene Glycol, TocopheryI Acetate (Vitamin E), Triethanolamine, Water(Aqua).
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