Data / Drug companies / Atlantis Consumer Healthcare, Inc.
Atlantis Consumer Healthcare, Inc.: 18 products in the FDA NDC directory, labeler code 67618
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Atlantis Consumer Healthcare, Inc. (labeler code 67618) lists 18 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 18 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on March 16, 2026.
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- Labeler code
- 67618
- Products in commercial distribution
- 18
- Packages
- 52
- Finished drugs by generic name
- 9
- Prescription products
- 0
- Over the counter products
- 18
- Flagged as original packager
- 17 of 17 products that carry the flag
- Started marketing in the last 12 months
- 2
- Earliest marketing start
- January 7, 1900
- 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 | 17 | 94.4% |
| New drug applications (NDA) | 1 | 5.6% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 18 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Povidone-iodine | 7 | 58 |
| Docusate sodium | 3 | 79 |
| Standardized senna concentrate | 2 | 3 |
| Docusate sodium - sennosides | 1 | 1 |
| Benzalkonium chloride | 1 | 271 |
| Benzalkonium cl and pramoxine hcl | 1 | 1 |
| Magnesium hydroxide | 1 | 41 |
| Antiseptic surgical scrub | 1 | 2 |
| Standardized senna concentrate and docusate sodium | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Solution | 7 | 38.9% |
| Tablet, film coated | 2 | 11.1% |
| Capsule | 2 | 11.1% |
| Capsule, liquid filled | 2 | 11.1% |
| Spray | 2 | 11.1% |
| Tablet | 2 | 11.1% |
| Aerosol, foam | 1 | 5.6% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Calculi Dissolution Agent | 1 |
| Osmotic Laxative | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Colace Fast-Acting Saline Laxative | 67618-102 | Capsule | Over the counter monograph drugs | March 16, 2026 |
| Betadine Foam Cleanser | 67618-184 | Aerosol, foam | Over the counter monograph drugs | February 1, 2026 |
| Betadine | 67618-190 | Solution | Over the counter monograph drugs | July 1, 2025 |
| Betadine | 67618-192 | Spray | Over the counter monograph drugs | January 2, 2025 |
| Colace extra strength stool softner | 67618-201 | Capsule, liquid filled | Over the counter monograph drugs | August 5, 2024 |
| Maximum Strength Betadine Clear | 67618-183 | Spray | Over the counter monograph drugs | December 22, 2023 |
| Betadine Gargle | 67618-181 | Solution | Over the counter monograph drugs | June 15, 2020 |
| Colace | 67618-101 | Capsule | Over the counter monograph drugs | January 30, 1997 |
| Betadine Surgical Scrub | 67618-151 | Solution | Over the counter monograph drugs | July 1, 1996 |
| Betasept | 67618-200 | Solution | New drug applications (NDA) | June 1, 1993 |
| Senokot | 67618-120 | Tablet, film coated | Over the counter monograph drugs | September 1, 1988 |
| Betadine Solution | 67618-150 | Solution | Over the counter monograph drugs | June 1, 1980 |
| Betadine Solution | 67618-150 | Solution | Over the counter monograph drugs | June 1, 1980 |
| Senokot-S | 67618-310 | Tablet | Over the counter monograph drugs | October 1, 1974 |
| Betadine Solution Swabsticks | 67618-153 | Solution | Over the counter monograph drugs | September 15, 1972 |
| Colace | 67618-110 | Tablet, film coated | Over the counter monograph drugs | February 8, 1957 |
| Senokot | 67618-300 | Tablet | Over the counter monograph drugs | June 1, 1956 |
| Colace | 67618-111 | Capsule, liquid filled | Over the counter monograph drugs | January 7, 1900 |
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.