Data / Drug companies / Elementis SRL, Inc.
Elementis SRL, Inc.: 55 products in the FDA NDC directory, labeler code 72450
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Elementis SRL, Inc. (labeler code 72450) lists 55 products in the FDA National Drug Code Directory. By type: 41 bulk ingredients, 14 drugs for further processing. Its main marketing category is bulk ingredients. The newest product started marketing on June 18, 2025.
The request: Watch Elementis SRL, Inc. (FDA labeler code 72450): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 72450
- Products in commercial distribution
- 55
- Packages
- 111
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- April 13, 2018
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Bulk ingredients | 41 | 74.5% |
| Drugs for further processing | 14 | 25.5% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 41 | 74.5% |
| Drugs for further processing | 14 | 25.5% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 41 | 74.5% |
| Solution | 14 | 25.5% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Aluminum zirconium pentachlorohydrex gly | 72450-997 | Powder | Bulk ingredients | June 18, 2025 |
| Aluminum zirconium tetrachlorohydrex gly | 72450-825 | Powder | Bulk ingredients | June 18, 2025 |
| Aluminum zirconium trichlorohydrex gly | 72450-824 | Powder | Bulk ingredients | June 18, 2025 |
| Aluminum zirconium tetrachlorohydrex gly | 72450-818 | Powder | Bulk ingredients | August 28, 2024 |
| Aluminum chlorohydrate | 72450-773 | Powder | Bulk ingredients | May 1, 2022 |
| Aluminum zirconium octachlorohydrex gly | 72450-772 | Powder | Bulk ingredients | June 1, 2021 |
| Aluminum zirconium tetrachlorohydrex gly | 72450-771 | Solution | Drugs for further processing | March 26, 2021 |
| Aluminum sesquichlorohydrate | 72450-770 | Powder | Bulk ingredients | December 2, 2020 |
| Aluminum chlorohydrate | 72450-769 | Powder | Bulk ingredients | October 1, 2020 |
| Aluminum chlorohydrate | 72450-768 | Powder | Bulk ingredients | June 12, 2020 |
| Aluminum chlorohydrate | 72450-766 | Powder | Bulk ingredients | May 1, 2020 |
| Aluminum chlorohydrate | 72450-763 | Solution | Drugs for further processing | October 1, 2019 |
| Aluminum chlorohydrate | 72450-100 | Solution | Drugs for further processing | August 1, 2019 |
| Aluminum sesquichlorohydrate | 72450-706 | Solution | Drugs for further processing | July 1, 2019 |
| Aluminum sesquichlorohydrate | 72450-703 | Powder | Bulk ingredients | July 1, 2019 |
| Aluminum chlorohydrate | 72450-762 | Powder | Bulk ingredients | April 1, 2019 |
| Aluminum zirconium tetrachlorohydrex gly | 72450-101 | Powder | Bulk ingredients | October 30, 2018 |
| Aluminum zirconium tetrachlorohydrex gly | 72450-754 | Solution | Drugs for further processing | April 13, 2018 |
| Aluminum zirconium pentachlorohydrate | 72450-751 | Solution | Drugs for further processing | April 13, 2018 |
| Aluminum zirconium tetrachlorohydrex gly | 72450-750 | Solution | Drugs for further processing | April 13, 2018 |
| Aluminum zirconium tetrachlorohydrex gly | 72450-748 | Powder | Bulk ingredients | April 13, 2018 |
| Aluminum zirconium octachlorohydrex gly | 72450-747 | Solution | Drugs for further processing | April 13, 2018 |
| Aluminum chlorohydrate | 72450-746 | Solution | Drugs for further processing | April 13, 2018 |
| Aluminum chlorohydrate | 72450-745 | Powder | Bulk ingredients | April 13, 2018 |
| Aluminum sesquichlorohydrate | 72450-743 | Solution | Drugs for further processing | April 13, 2018 |
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.