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Family Wellness

FDA UDI

Class I (US FDA UDI)

by Family Dollar Stores

Identity

Trade Name
Family Wellness FDA UDI
Generic Name
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free FDA UDI
Device Name
Denture Adhesive, Original FDA UDI
Model / Reference
QKA FDA UDI
Description
Denture Adhesive, Original FDA UDI

Identifiers

Primary DI / UDI-DI
00032251004278 FDA UDI
FDA Product Code
KOT 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-free

Family Wellness by Family Dollar Stores — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Family Dollar Stores

Sources (1)

  • FDA UDI a11f69c8-19d8-4a06-b101-4932ecf9a26d 33 fields · synced Jun 8, 2026