Data / Drug companies / Ingles Markets, Inc.
Ingles Markets, Inc.: 8 products in the FDA NDC directory, labeler code 62936
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Ingles Markets, Inc. (labeler code 62936) lists 8 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 8 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 1, 2026.
The request: Watch Ingles Markets, Inc. (FDA labeler code 62936): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 62936
- Products in commercial distribution
- 8
- Packages
- 13
- Finished drugs by generic name
- 5
- Prescription products
- 0
- Over the counter products
- 8
- Flagged as original packager
- 8 of 8 products that carry the flag
- Started marketing in the last 12 months
- 3
- Earliest marketing start
- January 1, 2004
- 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 | 7 | 87.5% |
| Generic drugs (ANDA) | 1 | 12.5% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 8 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Acetaminophen | 3 | 214 |
| Benzalkonium chloride | 2 | 271 |
| Alcohol | 1 | 293 |
| Ibuprofen | 1 | 190 |
| Acetaminophen, diphenhydramine hcl | 1 | 42 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 4 | 50% |
| Solution | 1 | 12.5% |
| Gel | 1 | 12.5% |
| Tablet, film coated | 1 | 12.5% |
| Liquid | 1 | 12.5% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Laura Lynn Moisturizing Advanced Gel Hand Sanitizer | 62936-0200 | Gel | Over the counter monograph drugs | July 1, 2026 |
| Laura Lynn Antibacterial Liquid Hand | 62936-0150 | Liquid | Over the counter monograph drugs | July 1, 2026 |
| Laura Lynn Foaming Fragrance and Dye Free Antibacterial Hand | 62936-0120 | Solution | Over the counter monograph drugs | July 1, 2026 |
| Extra Strength Pain Reliever | 62936-0219 | Tablet | Over the counter monograph drugs | November 1, 2024 |
| Extra Strength Pain Reliever PM | 62936-0224 | Tablet | Over the counter monograph drugs | July 1, 2024 |
| Regular Strength Pain Reliever | 62936-0102 | Tablet | Over the counter monograph drugs | June 1, 2019 |
| Extra Strength Pain Reliever | 62936-0222 | Tablet | Over the counter monograph drugs | August 1, 2018 |
| Ibuprofen | 62936-0941 | Tablet, film coated | Generic drugs (ANDA) | January 1, 2004 |
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.