Data / Drug companies / McKesson
McKesson: 57 products in the FDA NDC directory, labeler code 68599
McKesson (labeler code 68599) lists 57 products in the FDA National Drug Code Directory, covering 38 finished drugs by generic name. By type: 56 over the counter drugs, 1 prescription drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on April 23, 2026.
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- Labeler code
- 68599
- Products in commercial distribution
- 57
- Packages
- 104
- Finished drugs by generic name
- 38
- Prescription products
- 1
- Over the counter products
- 56
- Flagged as original packager
- 55 of 55 products that carry the flag
- Started marketing in the last 12 months
- 3
- Products with a marketing end date set
- 3
- Earliest marketing start
- April 9, 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 | 52 | 91.2% |
| New drug applications (NDA) | 2 | 3.5% |
| Generic drugs (ANDA) | 2 | 3.5% |
| Other unapproved drugs | 1 | 1.8% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 56 | 98.2% |
| Prescription drugs | 1 | 1.8% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Isopropyl alcohol | 5 | 177 |
| Ethanol | 4 | 8 |
| Povidone-iodine | 3 | 58 |
| Hydrogen peroxide | 2 | 100 |
| Benzalkonium chloride | 2 | 271 |
| Ethyl alcohol | 2 | 120 |
| Cough suppressant | 2 | 2 |
| Lanolin | 2 | 7 |
| Body cleanser | 2 | 1 |
| Aluminum chlorohydrate | 2 | 46 |
| Miconazole nitrate | 2 | 101 |
| Zinc oxide | 2 | 595 |
| Benzethonium chloride | 2 | 27 |
| Body shield | 1 | 1 |
| Antifungal | 1 | 6 |
| Benzocaine 20% | 1 | 5 |
| Menthol lozenge | 1 | 1 |
| Chlorhexidine gluconate | 1 | 34 |
| Skin protectant | 1 | 6 |
| Acetaminophen | 1 | 214 |
| Pain reliever | 1 | 2 |
| Bismuth subsalicylate | 1 | 80 |
| Loratainde | 1 | 1 |
| Chloroxylenol | 1 | 90 |
| Menthol | 1 | 263 |
| Calcium carbonate | 1 | 101 |
| Povidone iodine | 1 | 14 |
| Ibuprofen | 1 | 190 |
| Sodium fluoride | 1 | 124 |
| Silver nitrate | 1 | 7 |
| Aspirin | 1 | 134 |
| Phenylephrine hcl | 1 | 20 |
| Alcohol | 1 | 293 |
| Dimethicone | 1 | 69 |
| Lotionized hand sanitizer | 1 | 1 |
| Fluoride toothpaste | 1 | 3 |
| Purified water | 1 | 10 |
| Acetaminophen, phenylephrine hcl | 1 | 15 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Cream | 8 | 14% |
| Swab | 8 | 14% |
| Solution | 7 | 12.3% |
| Gel | 7 | 12.3% |
| Liquid | 7 | 12.3% |
| Lozenge | 4 | 7% |
| Tablet | 3 | 5.3% |
| Paste | 3 | 5.3% |
| Tablet, coated | 2 | 3.5% |
| Tablet, chewable | 2 | 3.5% |
| Tablet, film coated | 2 | 3.5% |
| Stick | 1 | 1.8% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Azole Antifungal | 3 |
| Nonsteroidal Anti-inflammatory Drug | 2 |
| alpha-1 Adrenergic Agonist | 2 |
| Standardized Chemical Allergen | 1 |
| Blood Coagulation Factor | 1 |
| Phosphate Binder | 1 |
| Platelet Aggregation Inhibitor | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Fluoride | 68599-9573 | Paste | Over the counter monograph drugs | April 23, 2026 |
| Fluoride | 68599-9571 | Paste | Over the counter monograph drugs | March 5, 2026 |
| Alcohol Prep Pad | 68599-5805 | Swab | Over the counter monograph drugs | January 14, 2026 |
| McKesson Loradatine | 68599-4785 | Tablet | Generic drugs (ANDA) | July 1, 2025 |
| Hand Sanitizer | 68599-5207 | Lotion | Over the counter monograph drugs | September 17, 2024 |
| McKesson Sinus Pain and Pressure Relief | 68599-4751 | Tablet | Over the counter monograph drugs | September 1, 2022 |
| McKesson Phenylephrine HCl | 68599-1631 | Tablet, film coated | Over the counter monograph drugs | September 1, 2022 |
| McKesson Sugar Free Cough Suppressant Oral Anesthetic | 68599-1090 | Lozenge | Over the counter monograph drugs | September 1, 2022 |
| McKesson Aspirin | 68599-1311 | Tablet, film coated | Over the counter monograph drugs | May 2, 2022 |
| McKesson Cough Supressant | 68599-0500 | Lozenge | Over the counter monograph drugs | May 2, 2022 |
| McKesson Bismuth | 68599-4744 | Tablet, chewable | Over the counter monograph drugs | March 1, 2022 |
| McKesson Orasol Gel | 68599-8247 | Gel | Over the counter monograph drugs | October 4, 2021 |
| McKesson Antiseptic Hand Sanitizer | 68599-1120 | Gel | Over the counter monograph drugs | October 4, 2021 |
| McKesson Ibuprofen 200 mg | 68599-8051 | Tablet, coated | Generic drugs (ANDA) | September 1, 2021 |
| McKesson Antacid Calcium Carbonate | 68599-1411 | Tablet, chewable | Over the counter monograph drugs | July 1, 2021 |
| McKesson Acetaminophen 325 | 68599-4679 | Tablet, coated | Over the counter monograph drugs | April 1, 2021 |
| Eye wash | 68599-1981 | Liquid | New drug applications (NDA) | April 1, 2021 |
| Swabs | 68599-6303 | Swab | Other unapproved drugs | April 21, 2020 |
| Instant Hand Sanitizing Wipe | 68599-5808 | Swab | Over the counter monograph drugs | February 24, 2020 |
| Acetaminophen | 68599-4681 | Tablet | Over the counter monograph drugs | January 30, 2020 |
| Menthol | 68599-0465 | Lozenge | Over the counter monograph drugs | January 30, 2020 |
| Menthol | 68599-0464 | Lozenge | Over the counter monograph drugs | January 29, 2020 |
| Dimethicone | 68599-0218 | Cream | Over the counter monograph drugs | November 4, 2019 |
| Dimethicone | 68599-0212 | Liquid | Over the counter monograph drugs | August 13, 2019 |
| Antimicrobial | 68599-0214 | Liquid | Over the counter monograph drugs | August 12, 2019 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). 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.