Is DENTAL TECHNOLOGIES, INC. FDA approved?

DENTAL TECHNOLOGIES, INC. holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are DENTAL TECHNOLOGIES, INC.'s drugs manufactured?

The FDA register lists LINCOLNWOOD, IL. Registered operations: labelling, finished drug manufacture, packaging, relabelling.

What drugs does DENTAL TECHNOLOGIES, INC. make?

20 products are listed under DENTAL TECHNOLOGIES, INC. in the openFDA NDC Directory, most often as gel; rinse. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

DENTAL TECHNOLOGIES, INC.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 20
Labeller names: 2
Live patents: 0
Countries: 1
Base: United States

Authorisation

Registered operations

Labelling1Finished drug manufacture1Packaging1Relabelling1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
DENTAL TECHNOLOGIES, INC.	6901 N. HAMLIN AVENUE, LINCOLNWOOD, Illinois (IL) 60712, United States (USA)	Labelling, Finished drug manufacture, Packaging, Relabelling	1413475148312838

Catalogue

Drug listings by form and route

20 active NDC listings: 18 human otc drug, 2 human prescription drug. By marketing category: OTC MONOGRAPH DRUG 18, UNAPPROVED DRUG OTHER 2.

Dosage form	NDCs
gel	19
rinse	1

Route	NDCs
dental	18
oral	5
periodontal	4
topical	1

Labeller name on the listing	NDCs
dental technologies, inc.	12
dental health products, inc.	8

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Alpha-Caine Topical Anesthetic	Benzocaine	gel, dental, periodontal	55346-2901OTC MONOGRAPH DRUG
Alpha-Caine Topical Anesthetic	Benzocaine	gel, dental, periodontal	55346-2902OTC MONOGRAPH DRUG
Alpha-Caine Topical Anesthetic	Benzocaine	gel, dental, periodontal	55346-2903OTC MONOGRAPH DRUG
Alpha-Caine Topical Anesthetic	Benzocaine	gel, dental, periodontal	55346-2904OTC MONOGRAPH DRUG
Alpha-Pro	Sodium Fluoride and Hydrofluoric Acid	gel, dental	55346-0942UNAPPROVED DRUG OTHER
Alpha-Pro	Sodium Fluoride and Hydrofluoric Acid	gel, dental	55346-0943UNAPPROVED DRUG OTHER
Health-Tec Topical Anesthetic	Benzocaine	gel, dental	69634-020OTC MONOGRAPH DRUG
Health-Tec Topical Anesthetic	Benzocaine	gel, dental	69634-021OTC MONOGRAPH DRUG
Health-Tec Topical Anesthetic	Benzocaine	gel, dental	69634-022OTC MONOGRAPH DRUG
Health-Tec Topical Anesthetic	Benzocaine	gel, dental	69634-023OTC MONOGRAPH DRUG
Health-Tec Topical Anesthetic	Benzocaine	gel, dental	69634-024OTC MONOGRAPH DRUG
Health-Tec Topical Anesthetic	Benzocaine	gel, dental	69634-025OTC MONOGRAPH DRUG
Health-Tec Topical Anesthetic	Benzocaine	gel, dental	69634-026OTC MONOGRAPH DRUG
Health-Tec Topical Anesthetic	Benzocaine	gel, dental	69634-027OTC MONOGRAPH DRUG
Home Care Fluoride	Stannous Fluoride	gel, dental, oral	55346-0401OTC MONOGRAPH DRUG
Home Care Fluoride	Stannous Fluoride	gel, dental, oral	55346-0402OTC MONOGRAPH DRUG
Home Care Fluoride	Stannous Fluoride	gel, dental, oral	55346-0404OTC MONOGRAPH DRUG
Home Care Fluoride	Stannous Fluoride	gel, dental, oral	55346-0408OTC MONOGRAPH DRUG
PEROXY SHIELD MOUTH SORE	1.5% Hydrogen Peroxide	rinse, oral	55346-3501OTC MONOGRAPH DRUG
San-EZ Hand Sanitizer	Ethyl Alcohol 70%	gel, topical	55346-3302OTC MONOGRAPH DRUG

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Enquiry

Common questions

Is DENTAL TECHNOLOGIES, INC. FDA approved?: DENTAL TECHNOLOGIES, INC. holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are DENTAL TECHNOLOGIES, INC.'s drugs manufactured?: The FDA register lists LINCOLNWOOD, IL. Registered operations: labelling, finished drug manufacture, packaging, relabelling.
What drugs does DENTAL TECHNOLOGIES, INC. make?: 20 products are listed under DENTAL TECHNOLOGIES, INC. in the openFDA NDC Directory, most often as gel; rinse. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.