Data / Drug companies / Troy Manufacturing, Inc.
Troy Manufacturing, Inc.: 20 products in the FDA NDC directory, labeler code 63936
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Troy Manufacturing, Inc. (labeler code 63936) lists 20 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 20 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on December 31, 2025.
The request: Watch Troy Manufacturing, Inc. (FDA labeler code 63936): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 63936
- Products in commercial distribution
- 20
- Packages
- 30
- Finished drugs by generic name
- 2
- Prescription products
- 0
- Over the counter products
- 20
- Flagged as original packager
- 19 of 19 products that carry the flag
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- October 13, 2010
- 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 | 18 | 90% |
| Unapproved homeopathic products | 2 | 10% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 20 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Menthol | 15 | 263 |
| Menthol, unspecified form | 3 | 30 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Gel | 15 | 75% |
| Liquid | 3 | 15% |
| Spray | 2 | 10% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Stopain Extra Strength Continuous | 63936-3850 | Spray | Over the counter monograph drugs | December 31, 2025 |
| Stopain Extra Strength Gel | 63936-8802 | Gel | Over the counter monograph drugs | June 15, 2025 |
| Ralli Rapid Pain Relief | 63936-9753 | Gel | Over the counter monograph drugs | February 1, 2024 |
| Ralli Rapid Pain Relief | 63936-9752 | Gel | Over the counter monograph drugs | February 1, 2024 |
| Ralli Rapid Pain Relief Roll on | 63936-9527 | Gel | Over the counter monograph drugs | February 1, 2024 |
| Ralli Rapid Pain Relief | 63936-9509 | Liquid | Over the counter monograph drugs | February 1, 2024 |
| Stopain Clinical | 63936-9751 | Gel | Over the counter monograph drugs | January 31, 2023 |
| Stopain Extra Strength | 63936-8801 | Gel | Over the counter monograph drugs | January 31, 2023 |
| Stopain Clinical | 63936-9758 | Gel | Over the counter monograph drugs | November 30, 2022 |
| Stopain Extra Strength Gel | 63936-8800 | Gel | Over the counter monograph drugs | October 10, 2022 |
| Stopain Extra Strength Gel | 63936-9506 | Gel | Over the counter monograph drugs | January 24, 2022 |
| Stopain Clinical | 63936-9505 | Gel | Over the counter monograph drugs | August 9, 2021 |
| Stopain Clinical Continuous | 63936-9504 | Liquid | Over the counter monograph drugs | January 1, 2020 |
| STOPAIN CLINICAL Migraine and Headache | 63936-9700 | Gel | Unapproved homeopathic products | July 1, 2018 |
| Stopain Extra Strength Continuous | 63936-4850 | Spray | Over the counter monograph drugs | April 1, 2018 |
| Stopain Clinical | 63936-0975 | Gel | Over the counter monograph drugs | January 19, 2017 |
| Stopain Clinical | 63936-9750 | Gel | Over the counter monograph drugs | January 18, 2017 |
| Stopain Clinical Roll-On | 63936-9520 | Gel | Over the counter monograph drugs | January 18, 2017 |
| Stopain Migraine Pain Relieving | 63936-8700 | Gel | Unapproved homeopathic products | March 20, 2015 |
| Extra strength stopain cold pain relieving roll on | 63936-8523 | Liquid | Over the counter monograph drugs | October 13, 2010 |
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.