Data / Drug companies / Wildman Business Group
Wildman Business Group: 14 products in the FDA NDC directory, labeler code 84269
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Wildman Business Group (labeler code 84269) lists 14 products in the FDA National Drug Code Directory, covering 13 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 January 16, 2026.
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- Labeler code
- 84269
- Products in commercial distribution
- 14
- Packages
- 21
- Finished drugs by generic name
- 13
- Prescription products
- 0
- Over the counter products
- 14
- Flagged as original packager
- 14 of 14 products that carry the flag
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- May 20, 2024
- 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 | 13 | 92.9% |
| Generic drugs (ANDA) | 1 | 7.1% |
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 |
|---|---|---|
| Acetaminophen, phenylephrine hydrochloride | 1 | 6 |
| Benzalkonium chloride, benzocaine | 1 | 5 |
| Magnesium salicylate | 1 | 4 |
| Hydrocortisone | 1 | 171 |
| Calcium carbonate | 1 | 101 |
| Isopropyl alcohol | 1 | 177 |
| Hydrogen peroxide | 1 | 100 |
| Acetaminophen | 1 | 214 |
| Caffeine, acetaminophen, aspirin | 1 | 1 |
| Lidocaine hydrochloride | 1 | 134 |
| Bacitracin zinc, neomycin sulfate, polymyxin b sulfate | 1 | 44 |
| Aspirin | 1 | 134 |
| Ibuprofen | 1 | 190 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 4 | 28.6% |
| Spray | 3 | 21.4% |
| Tablet, film coated | 2 | 14.3% |
| Cream | 1 | 7.1% |
| Capsule | 1 | 7.1% |
| Liquid | 1 | 7.1% |
| Ointment | 1 | 7.1% |
| Tablet, coated | 1 | 7.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Cherry Antacid | 84269-2517 | Tablet | Over the counter monograph drugs | January 16, 2026 |
| Hydrogen Peroxide | 84269-3503 | Spray | Over the counter monograph drugs | September 2, 2024 |
| Itch and Rash Cream | 84269-4506 | Cream | Over the counter monograph drugs | September 1, 2024 |
| Triple Antibiotic | 84269-4500 | Ointment | Over the counter monograph drugs | September 1, 2024 |
| Isopropyl Alcohol | 84269-3502 | Spray | Over the counter monograph drugs | September 1, 2024 |
| Antiseptic | 84269-3501 | Spray | Over the counter monograph drugs | September 1, 2024 |
| Lidocaine Hydrochloride | 84269-3500 | Liquid | Over the counter monograph drugs | September 1, 2024 |
| Ibuprofen | 84269-2525 | Tablet | Generic drugs (ANDA) | August 19, 2024 |
| Cold Terminator Cold Relief | 84269-2556 | Tablet, film coated | Over the counter monograph drugs | July 1, 2024 |
| Back Pain Relief Extra Strength Doans | 84269-2550 | Tablet, film coated | Over the counter monograph drugs | July 1, 2024 |
| Sinu-Phen Plus Sinus Pain and Pressure | 84269-2546 | Tablet | Over the counter monograph drugs | July 1, 2024 |
| Pain Terminator Extra Strength Pain Relief | 84269-2533 | Capsule | Over the counter monograph drugs | July 1, 2024 |
| Aspirin | 84269-2501 | Tablet, coated | Over the counter monograph drugs | July 1, 2024 |
| Acetaminophen | 84269-2522 | Tablet | Over the counter monograph drugs | May 20, 2024 |
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.