Data / Drug companies / Advantice Health, LLC
Advantice Health, LLC: 14 products in the FDA NDC directory, labeler code 16864
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Advantice Health, LLC (labeler code 16864) lists 14 products in the FDA National Drug Code Directory, covering 8 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 1, 2025.
The request: Watch Advantice Health, LLC (FDA labeler code 16864): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 16864
- Products in commercial distribution
- 14
- Packages
- 28
- Finished drugs by generic name
- 8
- 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
- 0
- Products with a marketing end date set
- 1
- Earliest marketing start
- January 1, 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 | 14 | 100% |
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 |
|---|---|---|
| Zinc oxide | 3 | 595 |
| Benzethonium chloride and benzocaine | 2 | 3 |
| Benzethonium chloride | 2 | 27 |
| Miconazole nitrate | 1 | 101 |
| Zinc oxide skin protectant | 1 | 1 |
| Benzocaine, menthol | 1 | 3 |
| Benzocaine and levomenthol | 1 | 1 |
| Benzocaine | 1 | 110 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Spray | 5 | 35.7% |
| Ointment | 4 | 28.6% |
| Powder, for solution | 2 | 14.3% |
| Paste | 1 | 7.1% |
| Liquid | 1 | 7.1% |
| Aerosol, spray | 1 | 7.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Standardized Chemical Allergen | 5 |
| Azole Antifungal | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Dermoplast Post Partum | 16864-640 | Aerosol, spray | Over the counter monograph drugs | January 1, 2025 |
| Multipurpose | 16864-041 | Ointment | Over the counter monograph drugs | September 16, 2024 |
| Triple 3x Max Diaper Rash | 16864-061 | Ointment | Over the counter monograph drugs | May 15, 2024 |
| Dermoplast Pain relieving | 16864-690 | Spray | Over the counter monograph drugs | March 18, 2022 |
| Dermoplast Kids First Aid | 16864-660 | Spray | Over the counter monograph drugs | March 1, 2022 |
| Triple Antifungal | 16864-040 | Ointment | Over the counter monograph drugs | September 1, 2021 |
| TriplePaste Adult Care Rash Treatment | 16864-031 | Paste | Over the counter monograph drugs | May 15, 2021 |
| Triple Diaper Rash | 16864-021 | Ointment | Over the counter monograph drugs | May 15, 2021 |
| Dermoplast Pain Relieving | 16864-680 | Spray | Over the counter monograph drugs | January 1, 2014 |
| Domeboro | 16864-240 | Powder, for solution | Over the counter monograph drugs | June 26, 2012 |
| Kerasal Athletes Foot Rapid Symptom Relief Medicated Soak | 16864-140 | Powder, for solution | Over the counter monograph drugs | June 26, 2012 |
| New Skin Bandage | 16864-450 | Spray | Over the counter monograph drugs | March 1, 2011 |
| New Skin Bandage | 16864-440 | Liquid | Over the counter monograph drugs | March 1, 2011 |
| Dermoplast First Aid | 16864-670 | Spray | Over the counter monograph drugs | January 1, 2010 |
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.