Data / Drug companies / MJ Products Association, LLC
MJ Products Association, LLC: 10 products in the FDA NDC directory, labeler code 72085
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
MJ Products Association, LLC (labeler code 72085) lists 10 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 10 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on August 10, 2020.
The request: Watch MJ Products Association, LLC (FDA labeler code 72085): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 72085
- Products in commercial distribution
- 10
- Packages
- 10
- Finished drugs by generic name
- 4
- Prescription products
- 0
- Over the counter products
- 10
- Flagged as original packager
- 10 of 10 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- March 1, 2018
- 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 | 10 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 10 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Homosalate, octocrylene, octisalate, zinc oxide | 4 | 2 |
| Octinoxate, octisalate, octocrylene, zinc oxide | 3 | 1 |
| Octinoxate, octocrylene, octisalate, avobenzone | 2 | 2 |
| Lidocaine hcl | 1 | 48 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Cream | 9 | 90% |
| Gel | 1 | 10% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Copper Absorption Inhibitor | 7 |
| Amide Local Anesthetic | 1 |
| Antiarrhythmic | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| BEACH GYPSY Glitter Sunscreen SPF 30 | 72085-312 | Cream | Over the counter monograph drugs | August 10, 2020 |
| SEA STAR SPARKLE SPF 50 Glitter Sunscreen Coco Lime | 72085-311 | Cream | Over the counter monograph drugs | August 10, 2020 |
| SEA STAR SPARKLE SPF 50 Glitter Sunscreen Coco Lime | 72085-309 | Cream | Over the counter monograph drugs | August 10, 2020 |
| SEA STAR SPARKLE SPF 50 Glitter Sunscreen Cotton Candy | 72085-308 | Cream | Over the counter monograph drugs | August 10, 2020 |
| SEA STAR SPARKLE SPF 50 Glitter Sunscreen Cotton Candy | 72085-307 | Cream | Over the counter monograph drugs | August 10, 2020 |
| Sea Star Sparkle SPF-50 VERY BERRY | 72085-149 | Cream | Over the counter monograph drugs | March 1, 2018 |
| Sea Star Sparkle SPF-50 PARTY CAKE | 72085-148 | Cream | Over the counter monograph drugs | March 1, 2018 |
| Sea Star Sparkle SPF-50 MANGO-TANGO | 72085-147 | Cream | Over the counter monograph drugs | March 1, 2018 |
| Beach Gypsy SPF-30 | 72085-146 | Cream | Over the counter monograph drugs | March 1, 2018 |
| Totally Fun After Sun | 72085-145 | Gel | Over the counter monograph drugs | March 1, 2018 |
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.