Data / Drug companies / Aluminum zirconium octachlorohydrex gly
Aluminum zirconium octachlorohydrex gly: 4 companies and 51 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Aluminum zirconium octachlorohydrex gly is listed in the FDA National Drug Code Directory by 4 companies, with 51 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are gel; liquid; cream, and the newest product started marketing on July 6, 2026.
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- Companies listing it
- 4
- Products
- 51
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 1
- Routes
- Topical
- Brand names
- Gillette ClearShield Sport Active Clear, Gillette ClearShield Arctic Ice Clear, Secret Relaxing Lavender Clear, Gillette ClearShield Pacific Tide Clear, Secret Outlast Hygienic Fresh Clear, Secret Tropical Hibiscus Clear, Gillette Clinical Protection Power Rush Clear, Secret Clinical Clear Clean Berry
- openFDA record search
- api.fda.gov
Companies that list aluminum zirconium octachlorohydrex gly
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| The Procter & Gamble Manufacturing Company | 43 | gel | Over the counter monograph drugs | July 6, 2026 |
| The Procter & Gamble Manufacturing Company | 6 | gel | Over the counter monograph drugs | May 1, 2023 |
| Clutch Inc | 1 | cream | Over the counter monograph drugs | June 1, 2020 |
| Highland Consumer Products | 1 | liquid | Over the counter monograph drugs | October 15, 2012 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Gel | 49 | 96.1% |
| Liquid | 1 | 2% |
| Cream | 1 | 2% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 51 | 100% |
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.