Hire the Best Best FDA Lawyer to Bring Your Hand Sanitizer to Market

The rise of COVID-19 has changed a lot in our world. The economy is free falling for some industries. Women are wearing less makeup because they don't leave the house as much and certainly don't need lipstick under a mask. People are going out to eat less. People are traveling less. People are wearing jeans less often. It's not gloom and doom, though. It's important to note that other companies are doing even better than before because they make products that are needed now more than ever. This includes hand sanitizer.

One of the best ways to prevent the spread of infections and decrease the risk of getting sick is by washing your hands with plain soap and water, according to the Centers for Disease Control and Prevention (CDC). Washing hands often with soap and water for at least 20 seconds is essential, especially after going to the bathroom; before eating; and after coughing, sneezing, or blowing one’s nose. Of course, people can't stop and wash their hands constantly. This is why hand sanitizer is booming in popularity. If soap and water are not available, CDC recommends consumers use an alcohol-based hand sanitizer that contains at least 60% alcohol.

It is important to note that people cannot make their own hand sanitizer. FDA does not recommend that consumers make their own hand sanitizer because, if made incorrectly, hand sanitizer can be ineffective. There have even been reports of skin burns from homemade hand sanitizer. If there is a product people need that they cannot make on their own, it means they are going to buy it. This translates to a lot of money to be made for companies like yours! It's time to hire the best FDA law firms to bring your hand sanitizer to market.

This isn't just a suggestion. If you don't have your hand sanitizer approved by the FDA, there could be serious consequences! The FDA and Federal Trade Commission (FTC) are taking actions against companies who make claims they cannot back up as part of their response in protecting Americans during the global COVID-19 outbreak. The FDA and the FTC issued warning letters to seven companies for selling fraudulent COVID-19 products. These products are unapproved drugs that pose significant risks to patient health and violate federal law. The warning letters were the first to be issued by the FDA for unapproved products intended to prevent or treat “Novel Coronavirus Disease 2019” (COVID-19). You don't want to be next on their list!

If you have any further questions or want to go through the process of having your product FDA approved for effectiveness against COVID-19, we recommend reaching out to the best FDA law firms. This professional will help you with everything you need to know and do to go to market. Soon, your profits will be soaring and you'll have no fear of the FDA sending you a warning letter because you'll know you're approved for market.