Data / Drug companies / R.L. Albert & Son, Inc
R.L. Albert & Son, Inc: 19 products in the FDA NDC directory, labeler code 83002
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
R.L. Albert & Son, Inc (labeler code 83002) lists 19 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 19 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on November 1, 2025.
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- Labeler code
- 83002
- Products in commercial distribution
- 19
- Packages
- 19
- Finished drugs by generic name
- 1
- Prescription products
- 0
- Over the counter products
- 19
- Flagged as original packager
- 19 of 19 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- November 15, 2022
- 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 | 19 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 19 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Menthol | 19 | 263 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Lozenge | 18 | 94.7% |
| Suspension/ drops | 1 | 5.3% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Menthol Drops Freegells Extra Strong Honey Lemon 30ct | 83002-012 | Lozenge | Over the counter monograph drugs | November 1, 2025 |
| Menthol Drops Freegells Extra Strong Eucalyptus 30ct | 83002-011 | Lozenge | Over the counter monograph drugs | November 1, 2025 |
| Freegells Cough Drops Honey Lemon 200ct | 83002-043 | Lozenge | Over the counter monograph drugs | March 15, 2024 |
| Freegells Cough Drops Menthol 80ct | 83002-042 | Lozenge | Over the counter monograph drugs | March 15, 2024 |
| Freegells Cough Drops Menthol 30ct | 83002-041 | Lozenge | Over the counter monograph drugs | March 15, 2024 |
| Freegells Cough Drops Menthol Cherry 30ct | 83002-040 | Lozenge | Over the counter monograph drugs | March 15, 2024 |
| Freegells Cough Drops Honey Lemon 30ct | 83002-039 | Lozenge | Over the counter monograph drugs | March 15, 2024 |
| Cough Drops Freegells Strawberry 30ct | 83002-038 | Lozenge | Over the counter monograph drugs | March 15, 2024 |
| Freegells Cough Drops Menthol Cherry 80ct | 83002-037 | Lozenge | Over the counter monograph drugs | March 15, 2024 |
| Cough Drops Freegells Strawberry 30ct | 83002-010 | Lozenge | Over the counter monograph drugs | July 14, 2023 |
| Freegells Cough Drops Menthol Honey Lemon 80ct | 83002-009 | Lozenge | Over the counter monograph drugs | July 5, 2023 |
| Freegells Cough Drops Menthol Cherry 200ct | 83002-008 | Lozenge | Over the counter monograph drugs | July 5, 2023 |
| Freegells Cough Drops Menthol Honey Lemon 200ct | 83002-007 | Lozenge | Over the counter monograph drugs | July 5, 2023 |
| Freegells Cough Drops Menthol Honey Lemon 30ct | 83002-006 | Lozenge | Over the counter monograph drugs | July 5, 2023 |
| Freegells Cough Drops Menthol 30ct | 83002-005 | Lozenge | Over the counter monograph drugs | July 5, 2023 |
| Freegells Cough Drops Menthol 80ct | 83002-004 | Lozenge | Over the counter monograph drugs | July 5, 2023 |
| Freegells Cough Drops Menthol Cherry 30ct | 83002-003 | Lozenge | Over the counter monograph drugs | July 5, 2023 |
| Freegells Cough Drops Menthol Cherry 80ct | 83002-002 | Lozenge | Over the counter monograph drugs | June 21, 2023 |
| Freegells cough drops menthol strawberry 30 drops | 83002-001 | Suspension/ drops | Over the counter monograph drugs | November 15, 2022 |
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.