Data / Drug companies / Product Max Group Inc
Product Max Group Inc: 11 products in the FDA NDC directory, labeler code 70742
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Product Max Group Inc (labeler code 70742) lists 11 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 11 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on February 28, 2025.
The request: Watch Product Max Group Inc (FDA labeler code 70742): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 70742
- Products in commercial distribution
- 11
- Packages
- 11
- Finished drugs by generic name
- 1
- Prescription products
- 0
- Over the counter products
- 11
- Flagged as original packager
- 11 of 11 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- November 18, 2017
- 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 | 11 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 11 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Benzocaine | 11 | 110 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Gel | 8 | 72.7% |
| Liquid | 3 | 27.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Standardized Chemical Allergen | 11 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Climax Shield Delay | 70742-598 | Liquid | Over the counter monograph drugs | February 28, 2025 |
| Thunder Fck Male Genital Desensitizer | 70742-587 | Liquid | Over the counter monograph drugs | February 13, 2025 |
| Body Action Climax Guard Delay | 70742-586 | Liquid | Over the counter monograph drugs | February 13, 2025 |
| BODY ACTION PRODUCTS Higher Control Male Climax | 70742-292 | Gel | Over the counter monograph drugs | April 29, 2022 |
| BODY ACTION PRODUCTS Prolong Lubricating | 70742-288 | Gel | Over the counter monograph drugs | April 29, 2022 |
| BODY ACTION PRODUCTS Anal Glide Extra | 70742-287 | Gel | Over the counter monograph drugs | April 29, 2022 |
| BODY ACTION PRODUCTS Butt Eze Benzocaine | 70742-286 | Gel | Over the counter monograph drugs | April 29, 2022 |
| BODY ACTION PRODUCTS Endless Love for Men | 70742-284 | Gel | Over the counter monograph drugs | April 29, 2022 |
| BODY ACTION PRODUCTS Climax Control Gel | 70742-282 | Gel | Over the counter monograph drugs | April 29, 2022 |
| HIGHER CONTROL Male Climax Control Lubricating | 70742-180 | Gel | Over the counter monograph drugs | March 1, 2018 |
| Endless Love For Men | 70742-360 | Gel | Over the counter monograph drugs | November 18, 2017 |
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.