Data / Drug companies / Gojo Industries, Inc.

Gojo Industries, Inc.: 85 products in the FDA NDC directory, labeler code 21749

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

Gojo Industries, Inc. (labeler code 21749) lists 85 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 85 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 31, 2026.

The request: Watch Gojo Industries, Inc. (FDA labeler code 21749): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code

21749

Products in commercial distribution

85

Packages

198

Finished drugs by generic name

7

Prescription products

0

Over the counter products

85

Flagged as original packager

85 of 85 products that carry the flag

Started marketing in the last 12 months

8

Products with a marketing end date set

2

Earliest marketing start

July 30, 1998

openFDA record search

api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Products by type

Drugs it lists

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

Dosage forms

Newest products

By marketing start date.

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.