Data / Drug companies / Strategic Sourcing Services LLC
Strategic Sourcing Services LLC: 35 products in the FDA NDC directory, labeler code 49348
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Strategic Sourcing Services LLC (labeler code 49348) lists 35 products in the FDA National Drug Code Directory, covering 30 finished drugs by generic name. By type: 35 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on January 1, 2016.
The request: Watch Strategic Sourcing Services LLC (FDA labeler code 49348): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 49348
- Products in commercial distribution
- 35
- Packages
- 40
- Finished drugs by generic name
- 30
- Prescription products
- 0
- Over the counter products
- 35
- Flagged as original packager
- 35 of 35 products that carry the flag
- Started marketing in the last 12 months
- 0
- Products with a marketing end date set
- 7
- Earliest marketing start
- October 3, 1989
- 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 | 30 | 85.7% |
| Generic drugs (ANDA) | 4 | 11.4% |
| Other unapproved drugs | 1 | 2.9% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 35 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Isopropyl alcohol | 3 | 177 |
| Miconazole nitrate | 2 | 101 |
| Loratadine and pseudoephedrine sulfate | 1 | 15 |
| Guaifenesin/phenylephrine | 1 | 7 |
| Polypropylene glycol 400, propylene glycol | 1 | 1 |
| Tetrahydrozoline hcl | 1 | 18 |
| Tolnaftate | 1 | 99 |
| Mineral oil | 1 | 34 |
| Calamine 8% and zinc oxide 8% | 1 | 11 |
| Glycerin, hypromellose, polyethylene glycol 400 | 1 | 13 |
| Hydrogen peroxide | 1 | 100 |
| Zinc acetate and pramoxine hydrochloride | 1 | 9 |
| Polyethylene glycol 400, propylene glycol | 1 | 25 |
| Witch hazel | 1 | 63 |
| Benzoin resin | 1 | 4 |
| Calamine and pramoxine hydrochloride | 1 | 7 |
| Hydrocortisone | 1 | 171 |
| Calamine and zinc oxide and phenol | 1 | 4 |
| Iodine, sodium iodide, alcohol | 1 | 1 |
| Dextran, polyethylene glycol 400, povidone, tetrahydrozoline | 1 | 1 |
| Ethyl alcohol | 1 | 120 |
| Aspirin | 1 | 134 |
| Phenazopyridine hydrochloride | 1 | 53 |
| Camphor 10% | 1 | 7 |
| Bacitracin zinc and polymyxin b sulfate | 1 | 9 |
| Povidone-iodine | 1 | 58 |
| Loratadine | 1 | 125 |
| Dextromethorphan hydrobromide / guaifenesin | 1 | 18 |
| Guaifenesin | 1 | 123 |
| Clotrimazole | 1 | 98 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Liquid | 8 | 22.9% |
| Solution/ drops | 5 | 14.3% |
| Tablet | 4 | 11.4% |
| Lotion | 4 | 11.4% |
| Cream | 3 | 8.6% |
| Ointment | 3 | 8.6% |
| Enema | 2 | 5.7% |
| Solution | 2 | 5.7% |
| Tablet, film coated, extended release | 1 | 2.9% |
| Tincture | 1 | 2.9% |
| Tablet, chewable | 1 | 2.9% |
| Suppository | 1 | 2.9% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Sunmark Witch Hazel | 49348-181 | Liquid | Over the counter monograph drugs | January 1, 2016 |
| Sunmark Hydrogen Peroxide 3 Percent | 49348-179 | Liquid | Over the counter monograph drugs | January 1, 2016 |
| Sunmark Isopropyl Alcohol 70 Percent With Wintergreen Oil | 49348-175 | Liquid | Over the counter monograph drugs | January 1, 2016 |
| Sunmark Isopropyl Alcohol 91 Percent | 49348-174 | Liquid | Over the counter monograph drugs | January 1, 2016 |
| Sunmark Urinary Pain Relief | 49348-076 | Tablet | Other unapproved drugs | July 1, 2013 |
| Sunmark Lubricating Tears | 49348-149 | Solution/ drops | Over the counter monograph drugs | May 1, 2013 |
| Sunmark Dry Eye Relief | 49348-095 | Solution/ drops | Over the counter monograph drugs | May 1, 2013 |
| Sunmark Saline Single Laxative | 49348-186 | Enema | Over the counter monograph drugs | March 6, 2013 |
| Chest Congestion Relief | 49348-729 | Tablet | Over the counter monograph drugs | August 1, 2012 |
| Sunmark Chest Congestion Relief DM DM | 49348-728 | Tablet | Over the counter monograph drugs | August 1, 2012 |
| Sunmark Povidone-Iodine Topical | 49348-622 | Solution | Over the counter monograph drugs | June 28, 2012 |
| Sunmark Iodine | 49348-133 | Tincture | Over the counter monograph drugs | June 28, 2012 |
| Sunmark Isopropyl Rubbing Alcohol | 49348-030 | Liquid | Over the counter monograph drugs | June 28, 2012 |
| Sunmark triple antibiotic plus pain relief | 49348-600 | Ointment | Over the counter monograph drugs | March 31, 2012 |
| Miconazole 7 | 49348-833 | Suppository | Generic drugs (ANDA) | December 9, 2011 |
| Sunmark Lubricant Eye Drops | 49348-947 | Solution/ drops | Over the counter monograph drugs | December 1, 2010 |
| Sunmark Iodides Tincture | 49348-711 | Liquid | Over the counter monograph drugs | January 1, 2008 |
| Sunmark Camphor Spirit | 49348-148 | Liquid | Over the counter monograph drugs | January 1, 2008 |
| Sunmark Benzoin Compound Tincture | 49348-138 | Liquid | Over the counter monograph drugs | January 1, 2008 |
| Sunmark Calamine | 49348-011 | Lotion | Over the counter monograph drugs | January 1, 2008 |
| Sunmark Eye Drops Advanced Moisturizer/Lubricant | 49348-697 | Solution/ drops | Over the counter monograph drugs | March 1, 2007 |
| Sunmark Eye Drops Original Formula | 49348-037 | Solution/ drops | Over the counter monograph drugs | March 1, 2007 |
| Sunmark Chest Congestion Relief PE PE | 49348-774 | Tablet | Over the counter monograph drugs | June 5, 2006 |
| Sunmark antifungal | 49348-155 | Cream | Over the counter monograph drugs | February 17, 2006 |
| Loratadine and Pseudoephedrine Sulfate | 49348-543 | Tablet, film coated, extended release | Generic drugs (ANDA) | November 17, 2004 |
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.