ANVEERUS Copper Ion Infused Face Mask is not a medical mask and not tested with Covid-19. This fabric face mask/cloth face cover are designed and intended for general public use only. They are not designed to be or replace any medical-grade PPE (Personal Protective Equipment). Be mindful when wearing mask if you have lung disease, like emphysema, or chronic heart disease. Stop using the mask if you notice breathing difficulty or skin sensitivity while wearing it. This mask is intended for adult use only. Children should be supervised by adult at all times when wearing a face mask to ensure safety. By choosing to wear the face mask we sell and/or distribute, an individual acknowledges and assumes all risks, known and unknown, associated therewith. The decision to use and wear our mask is solely your own. All images are for illustration purposes with approximate measurements. Actual products may vary due to product's enhancement. ANVEERUS Copper Ion Infused Face Mask and Pouch are hand-cut and sewn, please note that there may be slight differences between each piece, whilst maintaining the overall shape, fit and size. ANVEERUS Copper Mask Pouch is exclude of ANVEERUS Copper Ion Infused Face Mask. All ANVEERUS products are not exchangeable and/or refundable due to hygiene purpose.
Aqueous Ozone Sanitizing Spray Bottle has achieved a 99.9% virus reduction within 30 seconds against the commercial testing surrogate for Human Coronavirus SARS-CoV-2 (the virus that causes the CoVid-19 disease). The Enozo Spray Bottle was tested against surrogate 229E/ATCC VR-740 on hard non-porous surfaces using scientifically recognized testing methods.
Please note that the Enozo Aqueous Ozone Spray Bottle is categorized as a pesticidal device within the EPA classification structure. The EPA does not routinely include pesticidal devices in its review and therefore EPA has not confirmed whether, or under what circumstances, such products might be effective against the spread of COVID-19. Also, this explains why the Enozo sanitizing spray bottle does not qualify for listing with the chemical pesticidal formulations reviewed by EPA and included in EPA List N of disinfectants.
 Enozo Aqueous Ozone Spray Bottle is also branded by O3waterworks™ for U.S. consumer market
 Surrogate virus 229E/ATCC VR-740 is a commercially available virus that mimics the SARS-CoV-2 virus
 The test protocol is based in the ASTM E1052 Standard, with considerations for use of ozone.
The Enozo Aqueous Ozone Spray Bottle (also branded O3waterworks™) is classified as a pesticidal device under the EPA regulations. It has demonstrated effectiveness against viruses similar to SARS-CoV-2 (the virus causing COVID-19) on hard non-porous surfaces employing test methods recognized as scientifically valid in the field. However, it is important to note that unlike chemical pesticides, EPA does not routinely review the safety or efficacy of pesticidal devices, and therefore cannot confirm whether, or under what circumstances, such products might be effective against the spread of COVID-19.
By ordering and/or using the FEND products, you agree that you will follow all product directions. You agree that, to the fullest extent permitted by applicable law, in no event shall the FEND be liable for any indirect, special, incidental, consequential, exemplary, or punitive damages of any kind from the use or misuse of any product. FEND does not provide any medical advice along with the product, and the information provided should not be so construed or used. Using, accessing and/or browsing the product information does not create a physician-patient relationship, and no information is to replace the services of a licensed, trained physician or health professional or to be a substitute for medical or advice of a physician or trained health professional licensed in your state. You should not rely on anything contained about the product information and you should consult a physician licensed in your state in all matters related to your health. You hereby agree that you shall not make any health or medical related decisions based on whole or in part on information provided on FEND or along with the product.
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