NDC 68084-360-01 - Potassium 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
- 68084-360
- Requested NDC
- 68084-360-01
- Package NDCs from labels
- 68084-360-11, 68084-360-09, 68084-360-01
- Manufacturer
- American Health Packaging
- Effective date
- 2023-05-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Potassium Chloride - American Health Packaging | American Health Packaging | 2023-05-12 | 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 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68084-360-01 | EA - Each | 68084-360 | 1d087fdb-c5d3-480d-b073-1bbfac57e1e8 | 1 | 2012-07-24 |
| 68084-360-09 | EA - Each | 68084-360 | e1d842aa-7186-4525-99b1-c8c147388113 | 1 | 2016-02-04 |
| 68084-360-11 | EA - Each | 68084-360 | 866ecfee-212e-4497-a5f9-9ed1f616456e | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| POTASSIUM CHLORIDE | ACTIVE INGREDIENT | 660YQ98I10 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] | 2 | |
| POTASSIUM CATION | ACTIVE MOIETY | 295O53K152 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] | 2 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] | 2 | |
| DIETHYL PHTHALATE | INACTIVE INGREDIENT | UF064M00AF | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] | 2 | |
| ETHYLCELLULOSE (100 MPA.S) | INACTIVE INGREDIENT | 47MLB0F1MV | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] | 2 |
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 |
|---|---|---|---|---|---|---|
| Normosol-R | SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE | ICU Medical Inc. | 0e089a44-0cee-4804-8f6f-8508508ddb5c | 2025-10-30 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride in Dextrose | DEXTROSE MONOHYDRATE AND POTASSIUM CHLORIDE INJECTION, SOLUTION | ICU Medical Inc. | 02d694b5-3600-4d55-bd5c-924abaec5315 | 2025-10-30 | Warnings, Adverse reactions | 660YQ98I10 |
| Ionosol MB and Dextrose | DEXTROSE MONOHYDRATE, SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, POTASSIUM PHOSPHATE, MONOBASIC, AND SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE | ICU Medical Inc. | 1b457b1d-0e80-4578-ba6f-dedf513fc962 | 2025-10-30 | Warnings, Adverse reactions | 660YQ98I10 |
| Normosol-R | SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE | ICU Medical Inc. | 189b8ac6-e346-454f-b501-7645590ca4f8 | 2025-10-29 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride in Lactated Ringers and Dextrose | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE | Baxter Healthcare Corporation | 05f326e6-10e4-4ceb-8a23-f53c592f00b8 | 2025-10-29 | Warnings, Adverse reactions | 660YQ98I10 |
| Lactated Ringers and Dextrose | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE AND DEXTROSE MONOHYDRATE | Baxter Healthcare Corporation | 6acc9f96-7088-45a7-b48f-1a861e3467ab | 2025-10-29 | Warnings, Adverse reactions | 660YQ98I10 |
| Lactated Ringers | SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM LACTATE AND CALCIUM CHLORIDE | Baxter Healthcare Company | dad7735c-709b-40ea-ab7a-15577e24a966 | 2025-10-29 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride | POTASSIUM CHLORIDE | ICU Medical Inc. | eb56a807-ea94-4edb-9811-a04b19568468 | 2025-10-29 | Boxed warning, Warnings, Adverse reactions | 660YQ98I10 |
| Miranda Castros Healing Cell Salts For Bones, Hair, Nails, and Teeth | CALCAREA FLUORICA, CALCAREA PHOSPHORICA, SILICEA | MIRANDA CASTRO'S SHOP, LLC | 267fb775-a03c-f100-e063-6394a90aa826 | 2025-10-23 | Warnings | ETJ7Z6XBU4 |
| Miranda Castros healing cell salts for bones, hair, nails and teeth Homeopathic Combination | CALCAREA FLUORICA, CALCAREA PHOSPHORICA, SILICEA | MIRANDA CASTRO'S SHOP, LLC | 266e907b-4cdb-fb4f-e063-6394a90aa434 | 2025-10-23 | Warnings | ETJ7Z6XBU4 |
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE | ICU Medical Inc. | b96eb740-749a-4d3a-ae63-b8e3947cad30 | 2025-10-23 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium chloride | POTASSIUM CHLORIDE | Macleods Pharmaceuticals Limited | e0562a05-4359-4256-87e3-fcde65a008cd | 2025-10-18 | Warnings, Adverse reactions | 660YQ98I10 |
| Mold Relief Formula | KALI MURIATICUM, GELSEMIUM, KALI BICHROMICUM, SABADILLA, HISTAMINUM, MOLD MIX. | Integrative Healing Institute, LLC | 067ee707-7219-4370-9cdd-08888f45b5e5 | 2025-10-17 | Warnings | 660YQ98I10 |
| Seasonal Allergy Formula | HYDRASTIS CANADENSIS, KALI MURIATICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM, SABADILLA, HISTAMINUM, HOUSE DUST, GRASS MIX, TREES MIX, WEEDS MIX | Integrative Healing Institute, LLC | 1d4deee9-5452-421b-a107-ab150d1f6214 | 2025-10-17 | Warnings | 660YQ98I10 |
| KLOR-CON M | POTASSIUM CHLORIDE | Cardinal Health 107, LLC | ee3a1815-7325-4838-9764-fe1db68877b6 | 2025-10-17 | Warnings, Adverse reactions | 660YQ98I10 |
| DENTI BUONGIORNO PEACH MINT WHITENING TOOTH | HYDROGEN PEROXIDE, SILICA | ATOSAFE CO., Ltd | 41196c2f-8e2e-a54d-e063-6294a90ad8a7 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PEACH MINT WHITENING TOOTH | HYDROGEN PEROXIDE, SILICA | DONG IL PHARMS CO.,LTD | 41198822-7c8f-ceb2-e063-6394a90a4373 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO ORIGINAL TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 41197bb6-f6f4-c86d-e063-6294a90ad476 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO ORIGINAL TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | ATOSAFE CO., Ltd | 4114ab09-1115-6b0b-e063-6394a90ab442 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | ATOSAFE CO., Ltd | 41155922-d7ac-0a7a-e063-6294a90afe48 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.