Skip to the page

Data / Drug companies / Borden Company (Private) Limited

Borden Company (Private) Limited: 20 products in the FDA NDC directory, labeler code 43405

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

Borden Company (Private) Limited (labeler code 43405) lists 20 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 20 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on February 1, 2025.

The request: Watch Borden Company (Private) Limited (FDA labeler code 43405): 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
43405
Products in commercial distribution
20
Packages
36
Finished drugs by generic name
8
Prescription products
0
Over the counter products
20
Flagged as original packager
19 of 19 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
May 14, 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 drugs20100%

Products by type

TypeProductsShare
Over the counter drugs20100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Oil1365%
Liquid210%
Patch210%
Ointment210%
Liniment15%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Eagle Brand Medicated Plaster Extra Strength43405-301PatchOver the counter monograph drugsFebruary 1, 2025
Eagle Brand Medicated Roll On43405-016OilOver the counter monograph drugsJune 24, 2024
Eagle Brand Medicated Oil43405-015OilOver the counter monograph drugsJune 24, 2024
Eagle Brand Medicated Plaster43405-300PatchOver the counter monograph drugsFebruary 6, 2024
Eagle Brand Medicated Oil Aromatic43405-014OilOver the counter monograph drugsJanuary 9, 2024
Eagle Brand Medicated Oil Refresh43405-013OilOver the counter monograph drugsNovember 2, 2023
Eagle Brand Medicated Roll On Aromatic43405-017OilOver the counter monograph drugsNovember 1, 2023
Eagle Brand Medicated Roll On Refresh43405-012OilOver the counter monograph drugsNovember 1, 2023
Eagle Medicated43405-006OilOver the counter monograph drugsMarch 4, 2022
Eagle Medicated43405-005OilOver the counter monograph drugsMarch 4, 2022
Eagle Medicated Oil Refreshing43405-102OilOver the counter monograph drugsJune 30, 2021
Eagle Green Balm43405-100OintmentOver the counter monograph drugsMay 14, 2018
Eagle Brand Medicated Roll On Refresh43405-098OilOver the counter monograph drugsJuly 1, 2015
Eagle Brand Muscle Rub43405-096LinimentOver the counter monograph drugsJune 16, 2015
Eagle Brand Medicated Oil Aromatic43405-099OilOver the counter monograph drugsJune 15, 2015
Eagle Extra Strength43405-010LiquidOver the counter monograph drugsJune 15, 2015
Eagle Medicated Aromatic43405-009OilOver the counter monograph drugsJune 15, 2015
Eagle Brand Muscle Rub43405-011LiquidOver the counter monograph drugsMay 15, 2015
Eagle Medicated43405-008OilOver the counter monograph drugsMay 14, 2012
Muscular Balm43405-007OintmentOver the counter monograph drugsMay 14, 2010

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.