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Data / Drug companies / The Tetra Corporation

The Tetra Corporation: 5 products in the FDA NDC directory, labeler code 49406

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

The Tetra Corporation (labeler code 49406) lists 5 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 5 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 1, 2022.

The request: Watch The Tetra Corporation (FDA labeler code 49406): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
49406
Products in commercial distribution
5
Packages
5
Finished drugs by generic name
2
Prescription products
0
Over the counter products
5
Started marketing in the last 12 months
0
Earliest marketing start
October 30, 2012
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 drugs5100%

Products by type

TypeProductsShare
Over the counter drugs5100%

Drugs it lists

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

DrugProductsCompanies listing it
Tolnaftate499
Salicylic acid1330

Dosage forms

Dosage formProductsShare
Solution240%
Aerosol, foam120%
Liquid120%
Gel120%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
GlyCylic49406-009LiquidOver the counter monograph drugsJuly 1, 2022
FungiFoam49406-004Aerosol, foamOver the counter monograph drugsJuly 13, 2020
Formula 7 - The Solution49406-007SolutionOver the counter monograph drugsJune 13, 2018
Rapid MicroGel49406-005GelOver the counter monograph drugsJune 13, 2018
Formula 349406-003SolutionOver the counter monograph drugsOctober 30, 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.