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DawnMist

FDA UDI

Class I (US FDA UDI)

by Dukal LLC

Identity

Trade Name
DawnMist FDA UDI
Generic Name
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free FDA UDI
Device Name
Denture Adhesive Zinc Free 2.4 oz Tube FDA UDI
Model / Reference
DA2 FDA UDI
Description
Denture Adhesive Zinc Free 2.4 oz Tube FDA UDI

Identifiers

Catalog Number
DA2 FDA UDI
Primary DI / UDI-DI
00665973012902 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

Yes

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

Yes

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

DawnMist is a reliable and effective denture adhesive designed for use in removable prostheses, particularly dentures. This zinc-free, carboxymethylcellulose sodium/polymer denture adhesive is available in a convenient 2.4 oz tube and is suitable for daily wear. With its durable bond and long-lasting properties, DawnMist provides a comfortable and secure fit for users.

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
Dukal LLC

Sources (1)

  • FDA UDI 0ee9c035-af2d-42dc-90cf-adca35d71f3f 35 fields · synced Jun 26, 2026