Data / Drug companies / Sunset Novelties, Inc
Sunset Novelties, Inc: 15 products in the FDA NDC directory, labeler code 72937
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Sunset Novelties, Inc (labeler code 72937) lists 15 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 15 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on August 20, 2026.
The request: Watch Sunset Novelties, Inc (FDA labeler code 72937): 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
- 72937
- Products in commercial distribution
- 15
- Packages
- 18
- Finished drugs by generic name
- 4
- Prescription products
- 0
- Over the counter products
- 15
- Flagged as original packager
- 15 of 15 products that carry the flag
- Started marketing in the last 12 months
- 8
- Products with a marketing end date set
- 5
- Earliest marketing start
- May 24, 2019
- 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 | 15 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 15 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Menthol, camphor | 9 | 20 |
| Methyl salicylate, menthol | 3 | 15 |
| Menthol | 2 | 263 |
| Camphor | 1 | 23 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Cream | 9 | 60% |
| Gel | 6 | 40% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Menthol, camphor | 72937-013 | Cream | Over the counter monograph drugs | August 20, 2026 |
| Menthol, camphor | 72937-022 | Cream | Over the counter monograph drugs | February 12, 2026 |
| Cooling pain relief | 72937-629 | Gel | Over the counter monograph drugs | January 29, 2026 |
| Menthol, camphor | 72937-627 | Cream | Over the counter monograph drugs | January 29, 2026 |
| Heating pain relief | 72937-017 | Cream | Over the counter monograph drugs | January 29, 2026 |
| Menthol | 72937-632 | Gel | Over the counter monograph drugs | December 20, 2025 |
| Sunset heating pain relief roll-on | 72937-019 | Gel | Over the counter monograph drugs | December 2, 2025 |
| Sunset cooling pain relief roll-on | 72937-631 | Gel | Over the counter monograph drugs | December 1, 2025 |
| Cooling pain relief | 72937-630 | Gel | Over the counter monograph drugs | October 1, 2025 |
| Heating pain relief | 72937-018 | Cream | Over the counter monograph drugs | October 1, 2025 |
| Heating pain relief | 72937-180 | Cream | Over the counter monograph drugs | May 25, 2023 |
| Menthol, camphor | 72937-103 | Cream | Over the counter monograph drugs | October 5, 2020 |
| Menthol, camphor | 72937-006 | Gel | Over the counter monograph drugs | September 22, 2020 |
| Menthol, camphor | 72937-300 | Cream | Over the counter monograph drugs | February 4, 2020 |
| Menthol, camphor | 72937-010 | Cream | Over the counter monograph drugs | May 24, 2019 |
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.