FDA.reportPublic FDA data

NDC 66689-047-01 - 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
66689-047
Requested NDC
66689-047-01
Package NDCs from labels
66689-047-01, 66689-047-50, 66689-047-99, 66689-047-30, 66689-047-80
Manufacturer
VistaPharm, LLC
Effective date
2024-05-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Potassium Chloride - VistaPharm, LLCVistaPharm, LLC2024-05-09HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDCRelated label
66689-047-30These highlights do not include all the information needed to use POTASSIUM CHLORIDE safely and effectively. See full prescribing information for POTASSIUM CHLORIDE. POTASSIUM CHLORIDE oral solution Initial U.S. Approval: 1948
66689-047-50These highlights do not include all the information needed to use POTASSIUM CHLORIDE safely and effectively. See full prescribing information for POTASSIUM CHLORIDE. POTASSIUM CHLORIDE oral solution Initial U.S. Approval: 1948
66689-047-80These highlights do not include all the information needed to use POTASSIUM CHLORIDE safely and effectively. See full prescribing information for POTASSIUM CHLORIDE. POTASSIUM CHLORIDE oral solution Initial U.S. Approval: 1948
66689-047-99These highlights do not include all the information needed to use POTASSIUM CHLORIDE safely and effectively. See full prescribing information for POTASSIUM CHLORIDE. POTASSIUM CHLORIDE oral solution Initial U.S. Approval: 1948

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66689-047POTASSIUM CHLORIDE SOLUTION [VISTAPHARM, LLC]15Legacy NDC20240511_142c30ff-a839-4616-8167-ad4b07d8456f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66689-047-01ML - Milliliter66689-047bb1736ab-dff9-425e-96b9-0b14a2b2da9112016-03-04
66689-047-30ML - Milliliter66689-0479bfe89f8-8f34-4cb6-b8f3-2a4a4e298b6012017-07-07
66689-047-50ML - Milliliter66689-047dcc36d0c-834f-4de0-b82b-51b62fc79b1212016-03-04
66689-047-80ML - Milliliter66689-047729fbfda-64b8-4c88-ae26-404d0df09f6412017-07-07

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Potassium ChlorideACTIVE INGREDIENT660YQ98I10POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
Chloride IonACTIVE MOIETYQ32ZN48698POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
Anhydrous Citric AcidINACTIVE INGREDIENTXF417D3PSLPOTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
FD&C Yellow NO. 6INACTIVE INGREDIENTH77VEI93A8POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
GlycerinINACTIVE INGREDIENTPDC6A3C0OXPOTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
MethylparabenINACTIVE INGREDIENTA2I8C7HI9TPOTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
Propylene GlycolINACTIVE INGREDIENT6DC9Q167V3POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
PropylparabenINACTIVE INGREDIENTZ8IX2SC1OHPOTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
SucraloseINACTIVE INGREDIENT96K6UQ3ZD4POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
Trisodium Citrate DihydrateINACTIVE INGREDIENTB22547B95KPOTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]1
WaterINACTIVE INGREDIENT059QF0KO0RPOTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]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.

Matched openFDA labels page 45 of 52 · 1,026 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Emetrol Chewables Mixed BerrySODIUM CITRATE DIHYDRATEWellSpring Pharmaceutical Corporation4965fab0-828d-4f1d-8d43-a636e0a8c1ea2023-03-23WarningsExact identifier
unii: B22547B95K
Emetrol Chewables OrangeSODIUM CITRATE DIHYDRATEWellSpring Pharmaceutical Corporatione9072f9d-d74c-4e43-bcfe-ee005577df352023-03-23WarningsExact identifier
unii: B22547B95K
Myco Immuno NosodeDU HUO (ANGELICA PUBESCENS), ANGELICA ARCHANGELICA, KALI MURIATICUM, RADIX SILERIS (SAPOSHNIKOVIA DIVARICATA), YUCCA FILAMENTOSA, ACHYRANTHES BIDENTATA, ANGELICA SINENSIS, LIGUSTICUM PORTERI, PANAX GINSENG, RHUS TOX, HYDRASTIS CANADENSIS, UNCARIA TOMENTOSA, CARTILAGO SUIS, HORDEUM VULGARE, OXALICUM ACIDUM, ARNICA MONTANA, LATRODECTUS MACTANS, MAGNESIA PHOSPHORICA, MANGANUM METALLICUM, BORRELIA BURGDORFERI, BABESIA MICROTINutritional Specialties, Inc.34dc93af-0c39-4e06-a8d6-9e1ccc77aa232023-03-17WarningsExact identifier
unii: 660YQ98I10
Insulin Diluting Medium for NovoLogWATER INJECTIONNovo Nordisk3a1e73a2-3009-40d0-876c-b4cb2be56fc52023-02-28Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Potassium ChloridePOTASSIUM CHLORIDEFresenius Kabi USA, LLCfcd4f458-ce27-417e-9bb6-de1cc49d44b92023-02-27Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
triCitrasolTRISODIUM CITRATE DIHYDRATECitra Labs LLC64e7652c-1437-43bd-8ea2-3cafab447b8c2023-02-14Warnings, Adverse reactionsExact identifier
unii: B22547B95K
Anticoagulant Citrate Dextrose AANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATECitra Labs LLC5bcd261e-ebba-4ecb-af22-e5aaeb04499b2023-02-14Warnings, Adverse reactionsExact identifier
unii: XF417D3PSL
unii: B22547B95K
POLYETHYLENE GLYCOL-3350 AND ELECTROLYTESPOLYETHYLENE GLYCOL-3350 AND ELECTROLYTESNovel Laboratories, Inc.29d821ff-389c-41fb-8a27-89bd3f022b822023-02-08Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEA-S Medication Solutions87cc7349-5a07-4a39-be97-4e1013814f302023-02-06Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
POTASSIUM CHLORIDE EXTENDED RELEASEPOTASSIUM CHLORIDEGranules Pharmaceuticals Inc.9f8d2886-9ecd-4cbf-a84a-2d221cb3497c2023-01-27Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Kali muriaticumPOTASSIUM CHLORIDEBoiron8608d5a3-93e6-e8e2-e053-2a91aa0aaedc2023-01-23Exact identifier
unii: 660YQ98I10
Sodium Phenylacetate and Sodium BenzoateSODIUM PHENYLACETATE AND SODIUM BENZOATEMAIA PHARMACEUTICALSab40b62b-9f8d-4394-92d5-09d9f1941eaa2023-01-16Warnings, Adverse reactionsExact identifier
unii: OJ245FE5EU
CitriPlusJUGLANS REGIA WHOLE AND ANHYDROUS CITRIC ACIDPEKANA Natuheilmittel GmbH11db1b5b-2959-42c4-a059-25c9519330042023-01-11WarningsExact identifier
unii: XF417D3PSL
Ribotin-EFERROUS FUMARATE, FOLIC ACIDPureTek Corporationbb1492c5-bfcd-d632-e053-2a95a90ad7d12023-01-11Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Zintrexyl-CFERROUS FUMARATE, FOLIC ACIDPureTek Corporationbb1492c5-bfca-d632-e053-2a95a90ad7d12023-01-11Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
RehydrateAVENA SATIVA, EQUISETUM HYEMALE, HYPERICUM PERFORATUM, ULMUS FULVA, GLYCYRRHIZA GLABRA, SILICEA, PUERARIA LOBATA, CARLSBAD AQUA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, GERMANIUM SESQUIOXIDE, HYDROGEN, OXYGEN, WIESBADENParaDocs All Natural, Inc.648fab10-c46b-420f-a42c-6642009d83fb2023-01-10WarningsExact identifier
unii: 059QF0KO0R
Kali MurKALI MURIATICUMEnergique, Inc.db9894e6-2de0-428e-b553-11bb39a1d7112023-01-04WarningsExact identifier
unii: 660YQ98I10
GlucoregASCORBICUM ACIDUM, PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM, SARCOLACTICUM ACIDUM, THIAMINUM HYDROCHLORICUM, DHEA (DEHYDROEPIANDROSTERONE), PHLORIDZINUM, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALPHA-LIPOICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, NADIDUM, PANTOTHENIC ACID, ACETALDEHYDE, INSULINUM (SUIS), INSULINUM (HUMAN), HEPAR SUIS, PANCREAS SUIS, PHLORIDZINUM, BARYTA OXALICA, ALLOXANUM, BERBERIS VULGARIS, CARCINOSIN, LYCOPODIUM CLAVATUM, MOMORDICA BALSAMINA, PHOSPHORICUM ACIDUM, PHOSPHORUS,Deseret Biologicals, Inc.5117f980-95b8-4fc8-9425-8f6f056394372022-12-29WarningsExact identifier
unii: XF417D3PSL
KALI MURIATICUMPOTASSIUM CHLORIDEHyland's Inc.2e8a4762-d28d-4b64-892f-913e04d18d2d2022-12-19WarningsExact identifier
unii: 660YQ98I10
Dr Talbots Infant Pain Fever ReliefCALENDULA OFFICINALIS 12X,CHAMOMILLA 12X,ECHINACEA ANGUSTIFOLIA 12X,EUPATORIUM PERFOLIATUM 12X,HEPAR SULPHURIS CALCAREUM 12X,SULPHUR 12X,FERRUM PHOSPHORICUM 12X,KALI MURIATICUM 6XTalbot's Pharmaceuticals Family Products,LLC.e881a3ce-8cf9-0ce6-e053-2995a90ae8242022-12-16WarningsExact identifier
unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.