Skip to the page

Data / Drug companies / Ultradent Products, Inc.

Ultradent Products, Inc.: 10 products in the FDA NDC directory, labeler code 51206

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Ultradent Products, Inc. (labeler code 51206) lists 10 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 10 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 16, 2026.

The request: Watch Ultradent Products, Inc. (FDA labeler code 51206): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
51206
Products in commercial distribution
10
Packages
40
Finished drugs by generic name
4
Prescription products
0
Over the counter products
10
Flagged as original packager
7 of 7 products that carry the flag
Started marketing in the last 12 months
3
Products with a marketing end date set
7
Earliest marketing start
July 1, 1994
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs10100%

Products by type

TypeProductsShare
Over the counter drugs10100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Sodium fluoride4124
Potassium nitrate and sodium fluoride47
Opal by opalescence complete11
Opalescence whitening complete11

Dosage forms

Dosage formProductsShare
Gel, dentifrice10100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Opalescence Sensitivity Relief Whitening51206-451Gel, dentifriceOver the counter monograph drugsJuly 16, 2026
Opalescence Whitening Complete51206-452Gel, dentifriceOver the counter monograph drugsJune 25, 2026
Opalescence Whitening Original Cool Mint Cool Mint51206-450Gel, dentifriceOver the counter monograph drugsMay 13, 2026
Opalescence Whitening Sensitivity Relief51206-315Gel, dentifriceOver the counter monograph drugsOctober 8, 2025
Opalescence Whitening Cool Mint51206-314Gel, dentifriceOver the counter monograph drugsSeptember 23, 2025
Opal by Opalescence Complete51206-313Gel, dentifriceOver the counter monograph drugsOctober 21, 2024
Opal by Opalescence Original51206-312Gel, dentifriceOver the counter monograph drugsNovember 19, 2023
Opal by Opalescence Sensitivity51206-311Gel, dentifriceOver the counter monograph drugsNovember 19, 2023
Opalescence Sensitivity Relief Whitening51206-308Gel, dentifriceOver the counter monograph drugsNovember 30, 2015
Opalescence Whitening51206-302Gel, dentifriceOver the counter monograph drugsJuly 1, 1994

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.