Data / Drug companies / Uline
Uline: 16 products in the FDA NDC directory, labeler code 69790
Uline (labeler code 69790) lists 16 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 16 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on April 1, 2024.
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- Labeler code
- 69790
- Products in commercial distribution
- 16
- Packages
- 21
- Finished drugs by generic name
- 9
- Prescription products
- 0
- Over the counter products
- 16
- Flagged as original packager
- 14 of 14 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- January 19, 2015
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 13 | 81.2% |
| Generic drugs (ANDA) | 2 | 12.5% |
| New drug applications (NDA) | 1 | 6.2% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 16 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Alcohol | 3 | 293 |
| Acetaminophen | 3 | 214 |
| Benzalkonium chloride 0.13% | 2 | 19 |
| Ibuprofen | 2 | 190 |
| Benzalkonium chloride | 2 | 271 |
| Eyewash | 1 | 6 |
| Ethyl alcohol | 1 | 120 |
| Aspirin | 1 | 134 |
| Calcium carbonate | 1 | 101 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 4 | 25% |
| Soap | 3 | 18.8% |
| Liquid | 3 | 18.8% |
| Gel | 2 | 12.5% |
| Solution | 1 | 6.2% |
| Tablet, coated | 1 | 6.2% |
| Tablet | 1 | 6.2% |
| Tablet, chewable | 1 | 6.2% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 3 |
| Platelet Aggregation Inhibitor | 1 |
| Blood Coagulation Factor | 1 |
| Phosphate Binder | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| ULINE Eyewash | 69790-010 | Solution | New drug applications (NDA) | April 1, 2024 |
| Uline Acetaminophen Extra Strength | 69790-173 | Tablet, film coated | Over the counter monograph drugs | January 30, 2024 |
| Uline Acetaminophen Extra Strength | 69790-154 | Tablet, film coated | Over the counter monograph drugs | January 30, 2024 |
| Uline Ibuprofen | 69790-709 | Tablet | Generic drugs (ANDA) | April 4, 2022 |
| Uline Ibuprofen | 69790-609 | Tablet, coated | Generic drugs (ANDA) | April 4, 2022 |
| Hand Sanitizer | 69790-456 | Liquid | Over the counter monograph drugs | December 8, 2020 |
| ULINE Aspirin | 69790-616 | Tablet, film coated | Over the counter monograph drugs | July 20, 2020 |
| Uline Hand Sanitizer | 69790-801 | Gel | Over the counter monograph drugs | June 8, 2020 |
| Uline Antacid | 69790-820 | Tablet, chewable | Over the counter monograph drugs | October 7, 2019 |
| Uline Acetaminophen Extra Strength | 69790-804 | Tablet, film coated | Over the counter monograph drugs | October 7, 2019 |
| Alcohol | 69790-849 | Liquid | Over the counter monograph drugs | July 19, 2019 |
| Antibacterial Hand Wash | 69790-488 | Liquid | Over the counter monograph drugs | May 27, 2018 |
| Antibacterial | 69790-640 | Soap | Over the counter monograph drugs | September 12, 2017 |
| Hand Sanitizer | 69790-770 | Gel | Over the counter monograph drugs | March 28, 2016 |
| Hand Wash | 69790-466 | Soap | Over the counter monograph drugs | February 17, 2016 |
| Antibacterial | 69790-279 | Soap | Over the counter monograph drugs | January 19, 2015 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). 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.