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Data / Drug companies / Benco Dental

Benco Dental: 33 products in the FDA NDC directory, labeler code 66975

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

Benco Dental (labeler code 66975) lists 33 products in the FDA National Drug Code Directory, covering 14 finished drugs by generic name. By type: 18 over the counter drugs, 15 prescription drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on February 1, 2026.

The request: Watch Benco Dental (FDA labeler code 66975): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
66975
Products in commercial distribution
33
Packages
39
Finished drugs by generic name
14
Prescription products
15
Over the counter products
18
Flagged as original packager
33 of 33 products that carry the flag
Started marketing in the last 12 months
6
Products with a marketing end date set
1
Earliest marketing start
August 1, 2010
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 drugs1854.5%
Other unapproved drugs927.3%
Generic drugs (ANDA)412.1%
Authorized generics (NDA)26.1%

Products by type

TypeProductsShare
Over the counter drugs1854.5%
Prescription drugs1545.5%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Gel1854.5%
Paste, dentifrice618.2%
Injection, solution515.2%
Spray, metered13%
Soap13%
Rinse13%
Solution13%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Prosys66975-782Paste, dentifriceOther unapproved drugsFebruary 1, 2026
Pro-sys66975-780Paste, dentifriceOver the counter monograph drugsDecember 1, 2025
Pro-sys66975-779Paste, dentifriceOther unapproved drugsDecember 1, 2025
Pro-sys66975-778Paste, dentifriceOther unapproved drugsDecember 1, 2025
Pro-sys66975-720Paste, dentifriceOver the counter monograph drugsDecember 1, 2025
Pro-sys66975-700Paste, dentifriceOver the counter monograph drugsDecember 1, 2025
BencoCaine Topical Anesthetic66975-360Spray, meteredOver the counter monograph drugsDecember 1, 2021
BencoCaine Topical Anesthetic66975-343GelOver the counter monograph drugsOctober 1, 2020
BencoCaine Topical Anesthetic66975-341GelOver the counter monograph drugsOctober 1, 2020
BencoCaine Topical Anesthetic66975-340GelOver the counter monograph drugsOctober 1, 2020
Natural Extensions Antibacterial Foaming Hand66975-104SoapOver the counter monograph drugsNovember 15, 2018
Articaine66975-418Injection, solutionAuthorized generics (NDA)April 4, 2016
Articaine66975-417Injection, solutionAuthorized generics (NDA)April 4, 2016
Gibson Healthcare Buffered Hemostatic Solution66975-359SolutionOther unapproved drugsJanuary 1, 2015
BencoCaine Topical Anesthetic66975-358GelOver the counter monograph drugsJune 27, 2014
BencoCaine Topical Anesthetic66975-357GelOver the counter monograph drugsJune 27, 2014
BencoCaine Topical Anesthetic66975-356GelOver the counter monograph drugsJune 27, 2014
BencoCaine Topical Anesthetic66975-355GelOver the counter monograph drugsJune 27, 2014
BencoCaine Topical Anesthetic66975-354GelOver the counter monograph drugsJune 27, 2014
BencoCaine Topical Anesthetic66975-353GelOver the counter monograph drugsJune 27, 2014
BencoCaine Topical Anesthetic66975-352GelOver the counter monograph drugsJune 27, 2014
BencoCaine Topical Anesthetic66975-351GelOver the counter monograph drugsJune 27, 2014
BencoCaine Topical Anesthetic66975-350GelOver the counter monograph drugsJune 27, 2014
Iris 60 Second APF66975-054GelOther unapproved drugsDecember 14, 2012
Iris 60 Second APF66975-053GelOther unapproved drugsDecember 14, 2012

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.