NDC 79672-613-01 - Sodium Chloride
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
- 79672-613
- Requested NDC
- 79672-613-01
- Package NDCs from labels
- 79672-613-01, 79672-613-10, 79672-613-02, 79672-613-20, 79672-613-03, 79672-613-30, 79672-613-36, 79672-613-04, 79672-613-40, 79672-613-05, 79672-613-50
- Manufacturer
- Nextgen Pharmaceuticals LLC | LABORATORIOS GRIFOLS SA | Laboratorios Grifols, S. A.
- Effective date
- 2026-10-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 0.9% Sodium Chloride Injection, USP in FLEBOFLEX and FLEBOFLEX LUER Plastic Container | Nextgen Pharmaceuticals LLC | LABORATORIOS GRIFOLS SA | Laboratorios Grifols, S. A. | 2026-10-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79672-613-01 | Sodium Chloride | 50 mL in 1 BAG | INJECTION, SOLUTION | 50 | 12 | |
| 79672-613-02 | Sodium Chloride | 100 mL in 1 BAG | INJECTION, SOLUTION | 100 | 12 | |
| 79672-613-03 | Sodium Chloride | 250 mL in 1 BAG | INJECTION, SOLUTION | 250 | 12 | |
| 79672-613-04 | Sodium Chloride | 500 mL in 1 BAG | INJECTION, SOLUTION | 500 | 12 | |
| 79672-613-05 | Sodium Chloride | 1000 mL in 1 BAG | INJECTION, SOLUTION | 1000 | 12 | |
| 79672-613-10 | Sodium Chloride | 115 in 1 CARTON | INJECTION, SOLUTION | 115 | 12 | |
| 79672-613-20 | Sodium Chloride | 70 in 1 CARTON | INJECTION, SOLUTION | 70 | 12 | |
| 79672-613-30 | Sodium Chloride | 28 in 1 CARTON | INJECTION, SOLUTION | 28 | 12 | |
| 79672-613-40 | Sodium Chloride | 20 in 1 CARTON | INJECTION, SOLUTION | 20 | 12 | |
| 79672-613-50 | Sodium Chloride | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | 12 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 79672-613-01 | ML - Milliliter | 79672-613 | 56a381fe-9173-4a33-b103-47aa62579773 | 1 | 2021-05-05 |
| 79672-613-02 | ML - Milliliter | 79672-613 | 71794882-90fa-45e2-a5f2-7e36689af237 | 1 | 2021-05-05 |
| 79672-613-03 | ML - Milliliter | 79672-613 | 15c9bbf2-2ab1-4b4a-8e02-5d3ebb373649 | 1 | 2021-05-05 |
| 79672-613-04 | ML - Milliliter | 79672-613 | 2717138d-0631-4bef-b53c-b7d54d7aa2ab | 1 | 2021-05-05 |
| 79672-613-05 | ML - Milliliter | 79672-613 | 19bb89b7-a89a-423e-abad-20d97c42e4cf | 1 | 2021-05-05 |
| 79672-613-10 | ML - Milliliter | 79672-613 | e0bd4a04-98dd-4c8e-bb6d-225d539ee653 | 1 | 2021-05-05 |
| 79672-613-20 | ML - Milliliter | 79672-613 | fd20484f-d390-4884-8c57-c83f586155a6 | 1 | 2021-05-05 |
| 79672-613-30 | ML - Milliliter | 79672-613 | 28b7d4fc-57e8-46fe-860a-4e8aede1cdd7 | 1 | 2021-05-05 |
| 79672-613-40 | ML - Milliliter | 79672-613 | 66dea8e8-ed06-4b81-9e4c-bfc8b283911c | 1 | 2021-05-05 |
| 79672-613-50 | ML - Milliliter | 79672-613 | 32c61090-1410-4c30-85c7-0ff71f2e3c47 | 1 | 2021-05-05 |
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 |
|---|---|---|---|---|---|---|
| Potassium Chloride in Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, AND POTASSIUM CHLORIDE | Fresenius Kabi USA, LLC | 97001218-086c-430a-9e0d-6c7031c91d94 | 2024-05-06 | Warnings, Adverse reactions | 451W47IQ8X |
| Potassium Chloride in Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, AND POTASSIUM CHLORIDE | Fresenius Kabi USA, LLC | fe5b5182-c859-4c74-b2e0-467be5b2e329 | 2024-05-06 | Warnings, Adverse reactions | 451W47IQ8X |
| Sodium Chloride | SODIUM CHLORIDE | B. Braun Medical Inc. | f2475fa3-ab1d-4b81-8127-b58cd0790a54 | 2024-05-06 | Warnings, Adverse reactions | 451W47IQ8X |
| Weed Grass Antigens | ALLIUM CEPA, ARSENICUM ALBUM, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (PRATENSIS), ABROTANUM (ARTEMISIA ABROTANUM), ABSINTHIUM, AGRIMONIA EUPATORIA, FLOS, ALFALFA, AMBROSIA ARTEMISIAEFOLIA, ARUNDO MAURITANICA, BAMBUSA ARUNDINACEA, CICHORIUM INTYBUS, FLOS, KENTUCKY BLUEGRASS, ORCHARD GRASS, BERMUDA GRASS, JOHNSON GRASS, RYE GRASS, VERNAL GRASS, BAHIA GRASS, TIMOTHY GRASS, RUMEX CRISPUS, SABADILLA, SINAPIS ARVENSIS, FLOS, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE, TRIFOLIUM REPENS, | Energique, Inc. | 8a28f56a-6010-42e3-b360-e6e22b86222a | 2024-05-02 | Warnings | 451W47IQ8X |
| Potassium Chloride in Sodium Chloride | SODIUM CHLORIDE AND POTASSIUM CHLORIDE | Fresenius Kabi USA, LLC | c2467d57-cd2d-4409-bcc0-50128bd01bba | 2024-04-30 | Warnings, Adverse reactions | 451W47IQ8X |
| Mineffect eye drops | ALUMINA SILICATA, CALCAREA FLUORICA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, NATRUM MURIATICUM, PHOSPHORUS, SULPHUR, TITANIUM METALLICUM, ZINCUM METALLICUM | Kadesh Incoporation Co,Ltd | e2259f58-3043-4af3-918d-d4403757aa1f | 2024-04-26 | Warnings | 451W47IQ8X |
| LACTATED RINGERS | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE | Fresenius Kabi USA, LLC | 7a723a23-3bc1-4f69-b82f-d06a35dc68d6 | 2024-04-24 | Warnings, Adverse reactions | 451W47IQ8X |
| Sodium chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | c1e52670-c85e-4f19-a2e9-bf9abd7c3727 | 2024-04-23 | Warnings, Adverse reactions | 1807631 1807639 1807634 1807633 1807632 451W47IQ8X |
| PEMF Optimizer | AQUA SULIS, ARGENTUM METALLICUM, AURUM METALLICUM, CUPRUM METALLICUM, LAPIS ALBUS, MANGANUM METALLICUM VANADIUM METALLICUM VISCUM ALBUM, ZINCUM METALLICUM | Deseret Biologicals, Inc. | 97d57469-4c5b-4d3f-9398-3a1a6617a649 | 2024-04-23 | Warnings | 059QF0KO0R |
| Dermapar | EPIDERMIS (SUIS), ARSENICUM ALBUM, CALCAREA CARBONICA, GRAPHITES, MEZEREUM, NATRUM MURIATICUM, NITRICUM ACIDUM, PETROLEUM, RHUS TOX, SULPHUR, CAUSTICUM | Energique, Inc. | f79fe29b-341e-4bee-9665-1805a7157d1a | 2024-04-22 | Warnings | 451W47IQ8X |
| Sterile Water | WATER | Hikma Pharmaceuticals USA Inc. | 78ef7ad3-451d-43d0-a9b6-5cf0aadca003 | 2024-04-10 | Warnings, Adverse reactions | 059QF0KO0R |
| Sodium Chloride | SODIUM CHLORIDE | Hikma Pharmaceuticals USA Inc. | e5ee8caa-b6ca-45ba-98fb-8305e6282141 | 2024-04-10 | Adverse reactions | 451W47IQ8X |
| Sterile Water | WATER | B. Braun Medical Inc. | 8fc8d87a-3951-4ac5-97df-c161ffc90475 | 2024-04-10 | Warnings, Adverse reactions | 059QF0KO0R |
| Hers Plus | CALENDULA OFFICINALIS, SAMBUCUS NIGRA, ALLIUM SATIVUM, CLEMATIS ERECTA, DULCAMARA, SARSAPARILLA (SMILAX REGELII), GRAPHITES, PETROLEUM, ARSENICUM ALBUM, CROTON TIGLIUM, MERCURIUS SULPHURATUS RUBER, NATRUM MURIATICUM, NITRICUM ACIDUM, RHUS TOX, SEPIA, THUJA OCCIDENTALIS | Deseret Biologicals,Inc. | e4636b80-f6c8-459c-8d0e-ff7801358b10 | 2024-04-09 | Warnings | 451W47IQ8X |
| Dextrose And Sodium Chloride | DEXTROSE AND SODIUM CHLORIDE | B. Braun Medical Inc. | 8e6569ce-9714-497f-a94b-c6975c1d76f6 | 2024-04-02 | Warnings, Adverse reactions | 451W47IQ8X |
| SINU HC | PLANTAGO MAJOR, PULSATILLA (PRATENSIS), LUFFA OPERCULATA, MERCURIUS IODATUS RUBER, MUCOSA NASALIS SUIS, EUPHORBIUM OFFICINARUM, ARGENTUM NITRICUM, HEPAR SULPHURIS CALCAREUM, CALCAREA CARBONICA, NATRUM MURIATICUM, SINUSITISINUM | Deseret Biologicals, Inc. | 8b63e066-dd1b-4aee-a17b-4edc6b71a1cc | 2024-04-02 | Warnings | 451W47IQ8X |
| Eye Wash | WATER | M-star (Hubei) Health&Care Products Co., Ltd. | 71706039-e250-4f08-9687-71b2928c4e46 | 2024-04-01 | Warnings | 059QF0KO0R |
| CVS Health Sterile Saline Mist | SODIUM CHLORIDE | CVS Pharmacy | 14931004-1efb-e331-e063-6294a90ad66e | 2024-03-26 | Warnings | 451W47IQ8X |
| Aqua marina | SODIUM CHLORIDE | Boiron | 14945760-30b5-27d3-e063-6394a90a8a32 | 2024-03-26 | 451W47IQ8X | |
| Headache HP | BELLADONNA, BRYONIA, GELSEMIUM SEMPERVIRENS, GLONOINUM, MELILOTUS OFFICINALIS, NATRUM MURIATICUM | Energique, Inc. | 5dca8670-c931-47e3-af89-b5f09f5f4e02 | 2024-03-26 | Warnings | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.