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Data / Drug companies / Crosstex International Inc.

Crosstex International Inc.: 10 products in the FDA NDC directory, labeler code 24794

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

Crosstex International Inc. (labeler code 24794) lists 10 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 10 prescription drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on December 14, 2012.

The request: Watch Crosstex International Inc. (FDA labeler code 24794): 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
24794
Products in commercial distribution
10
Packages
10
Finished drugs by generic name
1
Prescription products
10
Over the counter products
0
Flagged as original packager
10 of 10 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
December 14, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Other unapproved drugs10100%

Products by type

TypeProductsShare
Prescription drugs10100%

Drugs it lists

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

DrugProductsCompanies listing it
Sodium fluoride10124

Dosage forms

Dosage formProductsShare
Gel10100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Zap APF24794-109GelOther unapproved drugsDecember 14, 2012
Zap Neutral24794-108GelOther unapproved drugsDecember 14, 2012
Zap APF24794-107GelOther unapproved drugsDecember 14, 2012
Zap APF24794-106GelOther unapproved drugsDecember 14, 2012
Zap APF24794-105GelOther unapproved drugsDecember 14, 2012
Zap APF24794-104GelOther unapproved drugsDecember 14, 2012
Zap APF24794-103GelOther unapproved drugsDecember 14, 2012
Zap APF24794-102GelOther unapproved drugsDecember 14, 2012
Zap APF24794-101GelOther unapproved drugsDecember 14, 2012
Zap APF24794-100GelOther 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.