Rexall QWC
Rexall QWC is a Class I device made by Dolgencorp, LLC, listed in FDA GUDID since 31 Aug 2020 (UDI-DI 00071031518543), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00071031518543 | Date31 Aug 2020 | StatusListed |
Official records
- AccessGUDID record 00071031518543
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Rexall
- Generic name
- Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free
- Model / reference
- QWC
- Primary DI / UDI-DI
- 00071031518543
- FDA product code
- KOT
- GMDN term
- Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free
- Device class
- Class I
- Regulation number
- 872.3490
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code KOT (Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium).
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