Periovance Dry Mouth Gel

Basic Information

• Brand Name: Periovance Dry Mouth Gel
• Primary DI: 00850058655086
• Version / Model: 7374-901P
• Company Name: ORABIO, INC.
• Labeler DUNS: 119105756
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2025-04-09
• Public Version: 2
• Public Version Date: 2025-06-11
• Public Version Status: Update
• Public Device Record Key: c00555d9-5818-42ca-801e-b8c468c36600

Device Description

Dry Mouth Gel - Mini

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
LFD	Saliva, Artificial	Unknown		U

GMDN Terms

Code	Name	Definition	Implantable	Status
37576	Artificial saliva	An electrolyte solution resembling human saliva designed in part to replace the normal ionic and pH balance of the oral cavity. The device is intended as a mouth rinse to moisten, lubricate, and clean the mucosa of the mouth, tongue, and throat. The device is indicated for dryness of the mouth or throat due to temporary or permanent conditions. After application, this device cannot be reused.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	00850058655109	GS1	Master Carton	100	In Commercial Distribution
Primary	00850058655086	GS1
Package	00850058655093	GS1	Case	10	In Commercial Distribution

Premarket Submissions

Submission Number	Supplement Number
K072306	000