Data / Drug companies / Quest Products, Inc.
Quest Products, Inc.: 14 products in the FDA NDC directory, labeler code 68229
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Quest Products, Inc. (labeler code 68229) lists 14 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 14 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on March 20, 2026.
The request: Watch Quest Products, Inc. (FDA labeler code 68229): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 68229
- Products in commercial distribution
- 14
- Packages
- 30
- Finished drugs by generic name
- 9
- Prescription products
- 0
- Over the counter products
- 14
- Flagged as original packager
- 13 of 13 products that carry the flag
- Started marketing in the last 12 months
- 2
- Earliest marketing start
- May 21, 2013
- 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 | 11 | 78.6% |
| Unapproved homeopathic products | 3 | 21.4% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 14 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Lidocaine hydrochloride and benzalkonium chloride | 5 | 2 |
| Lidocaine hydrochloride | 2 | 134 |
| Copper and arnica montana | 1 | 1 |
| Benzocaine | 1 | 110 |
| Calcium carbonate 250mg | 1 | 1 |
| Thuja occidentalis leafy twig | 1 | 6 |
| Calendula officinalis, grindelia robusta | 1 | 1 |
| Hydrocortisone 1% | 1 | 15 |
| Carbamide peroxide | 1 | 37 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Gel | 6 | 42.9% |
| Lozenge | 2 | 14.3% |
| Spray | 2 | 14.3% |
| Liquid | 2 | 14.3% |
| Ointment | 1 | 7.1% |
| Oil | 1 | 7.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Amide Local Anesthetic | 7 |
| Antiarrhythmic | 7 |
| Copper-containing Intrauterine Device | 1 |
| Standardized Chemical Allergen | 1 |
| Blood Coagulation Factor | 1 |
| Phosphate Binder | 1 |
| Corticosteroid | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Antacid Melts | 68229-800 | Lozenge | Over the counter monograph drugs | March 20, 2026 |
| Alocane Anti-Itch | 68229-411 | Gel | Over the counter monograph drugs | December 4, 2025 |
| Alocane Advanced Scar and Itch | 68229-409 | Gel | Unapproved homeopathic products | November 5, 2024 |
| SunBurnt PLUS | 68229-601 | Gel | Over the counter monograph drugs | February 23, 2024 |
| Alocane Max | 68229-408 | Spray | Over the counter monograph drugs | November 15, 2023 |
| Alocane Max | 68229-407 | Liquid | Over the counter monograph drugs | November 15, 2023 |
| CankerMelts | 68229-700 | Lozenge | Over the counter monograph drugs | October 6, 2023 |
| Alocane Botanicals | 68229-405 | Spray | Over the counter monograph drugs | August 11, 2023 |
| Clinere Ear Wax Remover | 68229-102 | Liquid | Over the counter monograph drugs | March 4, 2022 |
| Alocane Plus | 68229-404 | Gel | Over the counter monograph drugs | December 3, 2021 |
| Alocane Max | 68229-406 | Gel | Over the counter monograph drugs | May 1, 2020 |
| CopperFixx | 68229-502 | Ointment | Unapproved homeopathic products | January 1, 2016 |
| Alocane Plus | 68229-300 | Gel | Over the counter monograph drugs | December 11, 2013 |
| Skin Tag Relief | 68229-100 | Oil | Unapproved homeopathic products | May 21, 2013 |
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.