NDC 50844-417-43 - Naproxen Sodium
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 50844-417
- Requested NDC
- 50844-417-43
- Package NDCs from labels
- 50844-417-43, 50844-417-22, 50844-417-11, 50844-417-99, 50844-417-98, 50844-417-19, 50844-417-56, 50844-417-14, 50844-417-16
- Manufacturer
- L.N.K. International, Inc. | LNK International, Inc.
- Effective date
- 2026-02-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Quality Plus 44-417 and 44-604 | L.N.K. International, Inc. | LNK International, Inc. | 2026-02-25 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50844-417-11 | Naproxen Sodium | 60 in 1 CARTON | TABLET, FILM COATED | 60 | 15 | |
| 50844-417-14 | Naproxen Sodium | 500 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 500 | 15 | |
| 50844-417-16 | Naproxen Sodium | 1000 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 1000 | 15 | |
| 50844-417-19 | Naproxen Sodium | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 15 | |
| 50844-417-19 | Naproxen Sodium | 8 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 8 | 15 | |
| 50844-417-22 | Naproxen Sodium | 48 in 1 CARTON | TABLET, FILM COATED | 48 | 15 | |
| 50844-417-43 | Naproxen Sodium | 1 in 1 POUCH | TABLET, FILM COATED | 1 | 15 | |
| 50844-417-56 | Naproxen Sodium | 25 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 25 | 15 | |
| 50844-417-98 | Naproxen Sodium | 8 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 8 | 15 | |
| 50844-417-99 | Naproxen Sodium | 8 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 8 | 15 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Dolce and Gabbana Everlast Foundation SPF 20 03W Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 3b1e4480-8409-425e-b98d-eb4dcf2471e8 | 2025-08-04 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 06W Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 3090422e-fc18-45b8-88f2-6a9b282a7205 | 2025-08-04 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 05N Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | f93aa5d2-90ab-4e11-874e-2ede4b25c4b6 | 2025-08-04 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 04C Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | f055cd51-7b1d-43df-8990-8f60ba1eb91c | 2025-08-04 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 07N Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | d4c76bc5-205b-45fd-8a02-4f4b17458503 | 2025-08-04 | Warnings | 15FIX9V2JP |
| Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Kenvue Brands LLC | 003123d2-9675-fdd2-e063-6294a90a0130 | 2025-07-28 | Warnings | 15FIX9V2JP |
| Neutrogena Mineral Ultra Sheer Face SPF 70 | TITANIUM DIOXIDE, ZINC OXIDE | Kenvue Brands LLC | 20e0badf-fe25-1d27-e063-6294a90a7cfe | 2025-07-28 | Warnings | 15FIX9V2JP |
| Cell Salts | CALC. FLUOR., CALC. PHOS., CALC.SULPH., FERRUM PHOSPHORICUM, KALI MUR., KALI PHOS., KALI SULPH., MAG. PHOS., NAT. MUR., NAT. PHOS., NAT.SULPHURICUM, SILICEA | Newton Laboratories, Inc. | 985a3341-0fe0-1dd6-e053-2a95a90ad2c5 | 2025-07-25 | Warnings | ETJ7Z6XBU4 |
| Dolce and Gabbana Everlast Foundation SPF 20 01N Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 2ccf4e45-4cec-417d-9f4c-28f376025f1d | 2025-07-25 | Warnings | 15FIX9V2JP |
| SILICA MARINA | SILICON DIOXIDE | Boiron | 3aada26e-6a8e-f545-e063-6394a90a9f80 | 2025-07-24 | ETJ7Z6XBU4 | |
| Sunscreen | TITANIUM DIOXIDE 6.8% | Baxter of California, LLC | 146030bc-2bf4-25ea-e063-6294a90a4613 | 2025-07-24 | Warnings | 15FIX9V2JP |
| Cell Salts | CALC. FLUOR., CALC. PHOS., CALC.SULPH., FERRUM PHOSPHORICUM, KALI MUR., KALI PHOS., KALI SULPH., MAG. PHOS., NAT. MUR., NAT. PHOS., NAT.SULPHURICUM, SILICEA | Newton Laboratories, Inc. | 7a1b4e96-c96f-6424-e053-2991aa0aef30 | 2025-07-24 | Warnings | ETJ7Z6XBU4 |
| Cell Salts | CALC. FLUOR., CALC. PHOS., CALC.SULPH., FERRUM PHOSPHORICUM, KALI MUR., KALI PHOS., KALI SULPH., MAG. PHOS., NAT. MUR., NAT. PHOS., NAT.SULPHURICUM, SILICEA | Newton Laboratories, Inc. | 7a1a9ef9-9a54-5f94-e053-2a91aa0ab477 | 2025-07-24 | Warnings | ETJ7Z6XBU4 |
| Naproxen Sodium Caplets | NAPROXEN SODIUM | Dr Reddy's Laboratories Inc | ee0463bc-e939-1ecf-5a86-d045c426fecf | 2025-07-22 | Warnings | 849574 9TN87S3A3C |
| TopCare All Day Pain Relief | NAPROXEN SODIUM | Topco Associates LLC | 079eccdd-33bd-4b5c-bf46-9aef78559082 | 2025-07-22 | Warnings | 849574 9TN87S3A3C |
| Naproxen Sodium Headache Pain Caplets | NAPROXEN SODIUM | Dr.Reddy's Laboratories Inc | 605ca130-88aa-27d5-330c-6d9c95987f1f | 2025-07-22 | Warnings | 849574 9TN87S3A3C |
| Naproxen Sodium | NAPROXEN SODIUM | SAM'S WEST INC | 7a87a339-4482-ec9e-3c77-7ccb9cea2c4c | 2025-07-22 | Warnings | 849574 9TN87S3A3C |
| Naproxen Sodium | NAPROXEN SODIUM | Kroger Company | 30bcf289-0039-f389-73c4-fef3e8861034 | 2025-07-22 | Warnings | 849574 9TN87S3A3C |
| La Defense Broad Spectrum SPF 30 Mineral Sunscreen | ZINC OXIDE, TITANIUM DIOXIDE | Luzern Laboratories, Inc | 3f00befa-415d-415d-89e1-6ba8770ba51e | 2025-07-21 | Warnings | 15FIX9V2JP |
| Rugby Polyvinyl Alcohol 1.4% Lubricating Eye Drops | POLYVINYL ALCOHOL | A-S Medication Solutions | 2653e4fc-4f08-426d-a0a4-31d647c1de56 | 2025-07-18 | Warnings | 532B59J990 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.