Designed for smaller faces, this soft cotton mask has Adjustable ear loops and is shaped for a comfortable fit. Three-ply 100% combed ring spun cotton (Solids) Three-ply 50/50 combed ring spun cotton/poly (Heathers) Three-ply 90/10 combed ring spun cotton/poly (Light Heather Grey) Machine washable Gathers at nose and chin Non-medical use only Non-returnable Not a toy Not intended for children under age 4 Use under adult supervision only This product is not intended for use by health care professionals and is not intended as a replacement for personal protective equipment. This product makes no claims of antimicrobial protection, antiviral protection, particulate filtration or infection prevention or reduction. This product has not been FDA cleared or approved.
Designed for maximum comfort, the Port Authority® Cotton Knit Face Mask goes beyond standard cotton masks thanks to incorporation of Sciessent’s Agion® treatment into the fabric. Sciessent is a U.S.-based global provider of antimicrobial solutions and you can learn more about them here.
This three-ply, 100% cotton jersey face mask covers the wearer’s nose and mouth. Elastic stretch binding ear loops help hold it comfortably in place. Three-ply 100% cotton jersey Fabric touching skin: 100% cotton Mask contains silver and copper Three evenly-spaced pleats on each side May be used when FDA-cleared masks are unavailable Machine washable Non-returnable Not recommended for use in a surgical setting or where significant exposure to liquid, bodily or other hazardous fluids may be expected and where the infection risk level through inhalation exposure is high. The product has not been FDA cleared or approved. The product has been authorized by FDA under an EUA for use by HCP as PPE to help prevent the spread of infection or illness in healthcare settings and by the general public to help slow the spread of the virus during the COVID-19 pandemic. This product is authorized only for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of medical devices, including alternative products used as medical devices, during the COVID-19 outbreak, under section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1) unless the authorization is terminated or revoked sooner.