Efficacy of VRx MyBiotics Oral Lozenges

This is a single arm, interventional trial on adults residing in the United States. The study will test the efficacy of personalized oral biotic lozenges (VRx MyBiotics Oral Lozenges) at improving oral microbiome health according to Viome's Oral Health Score.

Inclusion criteria

• Any person with a US address that is 18 years old or older
• Able to speak and read English
• Willing and able to follow the trial instructions, as described in the recruitment letter
• Signed and dated informed consent prior to any trial-specific procedures.

Exclusion criteria

• Systemic antibiotic treatment 30 days prior to enrollment or during the trial
• Not willing to stop sporadic use (less frequently than daily) of any mouthwash.
• Significant diet, supplements, or lifestyle change in the previous 1 month or next 2 months once enrolled
• Allergy to tapioca, peppermint, or sweet potato
• Current diagnosis of periodontitis or other advanced oral disease (chronic recurrent caries, oral cancer, etc)
• No dental procedures 30 days prior to enrollment or during the trial (regular cleanings, bone grafts, dental implants, etc)
• Pregnancy or planned pregnancy
• Currently have cancer or undergoing cancer therapy
• Dentures
• Fewer than 20 teeth
• Use of at home teeth whitening products 30 days prior to enrollment or during the trial
• Start new medications or supplements during the trial