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DawnMist DA2

by Dukal LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Overview

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.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00665973012902 UDI-DI Date6 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
DawnMist
Generic name
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free
Model / Ref / Catalog
DA2
Primary DI / UDI-DI
00665973012902
FDA product code
KOO
GMDN term
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free
Device class
Class I
Regulation number
872.3490
GUDID distribution status
In Commercial Distribution

Related devices

Category: Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free

Similar devices

Other devices filed under FDA product code KOO (ADHESIVE, DENTURE, POLYVINYL METHYLETHER MALEIC ACID CALCIUM-SODIUM DOUBLE SALT).

Other devices from Dukal LLC

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Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)