Identity
- Trade Name
- DG Health FDA UDI
- Generic Name
- Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free FDA UDI
- Device Name
- Denture Adhesive, Super Item No. 13625601 FDA UDI
- Model / Reference
- TPE FDA UDI
- Description
- Denture Adhesive, Super Item No. 13625601 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00857331000021 FDA UDI
- FDA Product Code
- KOO FDA UDI
- GMDN Term
- Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3490 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Carboxymethylcellulose sodium/polymer denture adhesive, zinc-freePolyvinyl methylether maleic acid calcium-sodium double salt denture adhesive
DG Health by Dolgencorp, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Polyvinyl methylether maleic acid calcium-sodium double salt denture adhesive.
- Dyna Care Denture Adhesive — Dynarex Corp. · Class I
- Rexall — DOLGENCORP, LLC · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Dolgencorp, Llc
Sources (1)
- FDA UDI 199631b7-6928-4946-b07e-981763ea8f09 33 fields · synced Jun 6, 2026