Rexall

GUDID 10071031517543

Denture Adhesive, Super

DOLGENCORP, LLC

Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free

• Primary Device ID: 10071031517543
• NIH Device Record Key: 18a73a17-ee37-4355-acda-fd37e28ecb30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rexall
• Version Model Number: TPE
• Company DUNS: 068331990
• Company Name: DOLGENCORP, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00071031517546 [Primary]
GS1	10071031517543 [Package]; Contains: 00071031517546; Package: case [48 Units]; In Commercial Distribution

FDA Product Code

• KOT: Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-08
• Device Publish Date: 2020-08-31

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