NDC 31722-341-01 - Naproxen
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
- 31722-341
- Requested NDC
- 31722-341-01
- Package NDCs from labels
- 31722-341-10, 31722-341-50, 31722-341-01, 31722-341-05
- Manufacturer
- Camber Pharmaceuticals | Invagen Pharmaceuticals
- Effective date
- 2025-09-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Naproxen - Camber Pharmaceuticals | Invagen Pharmaceuticals | Camber Pharmaceuticals | Invagen Pharmaceuticals | 2025-09-03 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 31722-341-05 | 2025-09-05 | Naproxen Tablets, USP |
| 31722-341-50 | 2025-09-05 | Naproxen Tablets, USP |
| 31722-341-05 | 2019-11-13 | Naproxen Tablets, USP |
| 31722-341-50 | 2019-11-13 | Naproxen Tablets, USP |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 31722-341-01 | EA - Each | 31722-341 | 63b4f6d3-ac77-44dc-968a-b2227779ca6c | 1 | 2012-07-24 |
| 31722-341-05 | EA - Each | 31722-341 | a8f53f56-e3c1-48dd-b586-26588e68d297 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| NAPROXEN | ACTIVE INGREDIENT | 57Y76R9ATQ | NAPROXEN TABLET [CAMBER PHARMACEUTICALS] | 1 | |
| NAPROXEN | ACTIVE MOIETY | 57Y76R9ATQ | NAPROXEN TABLET [CAMBER PHARMACEUTICALS] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | NAPROXEN TABLET [CAMBER PHARMACEUTICALS] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | NAPROXEN TABLET [CAMBER PHARMACEUTICALS] | 1 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | NAPROXEN TABLET [CAMBER PHARMACEUTICALS] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NAPROXEN TABLET [CAMBER PHARMACEUTICALS] | 1 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | NAPROXEN TABLET [CAMBER PHARMACEUTICALS] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | NAPROXEN TABLET [CAMBER PHARMACEUTICALS] | 1 |
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 |
|---|---|---|---|---|---|---|
| MINIDROPS | LUBRICANT EYE DROPS | Optics Laboratory, Inc | c13c5f91-50df-471c-a7c9-1747a2ac1250 | 2026-02-03 | Warnings | FZ989GH94E |
| Mold, Yeast and Dust | ACREMONIUM STRICTUM, ADRENALINUM, ALLIUM CEPA, ALTERNARIA ALTERNATA, ARSENICUM IODATUM, ASPERGILLUS FUMIGATUS, ASPERGILLUS NIGER, AUREOBASIDIUM PULLULANS, CANDIDA ALBICANS, CLADOSPORIUM HERBARUM, COCKROACH, DERMATOPHAGOIDES FARINAE, EPICOCCUM PURPURASCENS, FUSARIUM SOLANI, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, MUCOR CIRCINELLOIDES, NATRUM SULPHURICUM, RHIZOPUS STOLONIFER, SACCHAROMYCES CEREVISIAE, SILICEA | NaturalCare | e0f53f47-acd9-43e2-a7a2-2a500bc9dc1b | 2026-02-03 | Warnings | ETJ7Z6XBU4 |
| Aquavit 1 | AQUAVIT 1 | Uriel Pharmacy Inc. | 2354fcfc-05a2-444a-ace4-b3df61413157 | 2026-02-02 | Warnings | 1K09F3G675 |
| Naproxen | NAPROXEN | A-S Medication Solutions | 4e97e645-552d-424b-990a-f94349a86f17 | 2026-01-30 | Boxed warning, Warnings, Adverse reactions | 57Y76R9ATQ |
| Calamine | CALAMINE | AMERISOURCE BERGEN | 90d9d908-57ea-4062-ade0-8a4888939c91 | 2026-01-29 | Warnings, Adverse reactions | 1K09F3G675 |
| Naproxen | NAPROXEN | A-S Medication Solutions | 000155a8-709c-44e5-a75f-cd890f3a7caf | 2026-01-29 | Boxed warning, Warnings, Adverse reactions | 57Y76R9ATQ |
| Naproxen | NAPROXEN | A-S Medication Solutions | d06db628-f6f0-48e2-b538-69c0837c49e3 | 2026-01-29 | Boxed warning, Warnings, Adverse reactions | 57Y76R9ATQ |
| Naproxen | NAPROXEN | A-S Medication Solutions | 9d28422f-6f25-4f14-9272-e0907c971f33 | 2026-01-29 | Boxed warning, Warnings, Adverse reactions | 57Y76R9ATQ |
| Naproxen | NAPROXEN | Preferred Pharmaceuticals Inc. | 87acd650-ea8a-4396-be72-5568c4b1755c | 2026-01-23 | Boxed warning, Warnings, Adverse reactions | 57Y76R9ATQ |
| BioMicroneedle PDRN Cream | SILICON DIOXIDE | Guangzhou Shengyanghui Industrial Trading Co., Ltd | 48e2edae-94ea-c42e-e063-6394a90a907b | 2026-01-21 | Warnings | ETJ7Z6XBU4 |
| Inflammation I | ECHINACEA (ANGUSTIFOLIA), NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, APIS MELLIFICA, BELLADONNA, FERRUM PHOSPHORICUM, NITRICUM ACIDUM, OLEANDER, SILICEA | BioActive Nutritional, Inc. | 3cb12181-ae7e-45c7-a1b1-e1952f36f8c3 | 2026-01-21 | Warnings | ETJ7Z6XBU4 |
| Naproxen and esomeprazole magnesium | NAPROXEN AND ESOMEPRAZOLE MAGNESIUM | Preferred Pharmaceuticals Inc. | b295a90e-320f-4414-b80a-d11f06c00c96 | 2026-01-20 | Boxed warning, Warnings, Adverse reactions | 57Y76R9ATQ |
| DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | ATOSAFE CO., Ltd | 487c5036-0eb0-ada9-e063-6394a90aa02e | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | DONG IL PHARMS CO.,LTD | 487cd5b9-28f3-392d-e063-6394a90a9ba1 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | ATOSAFE CO., Ltd | 487cf27a-d761-6353-e063-6394a90af029 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | ATOSAFE CO., Ltd | 487d52d1-8853-bc90-e063-6394a90ab91d | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | DONG IL PHARMS CO.,LTD | 487d689d-ebdd-43c3-e063-6294a90af0e2 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 487da363-1d01-8cdc-e063-6294a90ac24d | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| Berberis Quartz | BERBERIS QUARTZ | Uriel Pharmacy Inc. | 5da48d70-1140-495d-b672-0e55c04196e1 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| Constipation Relief | ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE | Homeocare Laboratories | 62374240-cd14-44e2-9405-5f8996faf047 | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.