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 16 of 54 · 1,062 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BM Kali Mur Icing SugarKALIUM MURIATICUM ICING SUGARBM Private Limited37c3c5c0-ab13-5e8a-e063-6394a90a786b2025-12-02WarningsExact identifier
unii: 660YQ98I10
BUDDATE INONOTUS OBLIQUUS WATER BRILLIANCE MASKBUTYLENE GLYCOL, GLYCERIN, INONOTUS OBLIQUUS (MUSHROOM) EXTRACTBUDDATE Co Ltd464988ad-557e-13f5-e054-00144ff8d46c2025-11-30WarningsExact identifier
unii: PDC6A3C0OX
BUDDATE LOTUS MOISTURE ESSENCEGLYCERIN, NIACINAMIDE, NELUMBO NUCIFERA FLOWER EXTRACT, PORTULACA OLERACEA EXTRACTBUDDATE Co Ltd46499995-8b13-3e5c-e054-00144ff88e882025-11-30WarningsExact identifier
unii: PDC6A3C0OX
Potassium Chloride ERPOTASSIUM CHLORIDE ERDirect_Rx42c92fcc-21d2-d32a-e063-6294a90a83122025-11-26Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
ACD-AANTICOAGULANT CITRATE DEXTROSE SOLUTION FORMULA AFenwal, Inc.ab19b011-0a51-4f04-9881-d9fc7cae95ae2025-11-25Exact identifier
unii: XF417D3PSL
Potassium chloridePOTASSIUM CHLORIDEAphena Pharma Solutions - Tennessee, LLC42773f05-7c2c-1790-e063-6294a90a78b32025-11-24Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
PUR-WASHWATERNiagara Pharmaceuticals Inc.beda35c3-9a8b-47ad-e053-2995a90a7b1b2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Easy Care First Aid EyewashWATERTender Corporationa070aac8-e6d2-ef10-e053-2a95a90aa5b12025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.e07a064b-f680-405c-bbcd-24fac430951e2025-11-24WarningsExact identifier
unii: 059QF0KO0R
ULINE EyewashEYEWASHNiagara Pharmaceuticals Inc.2d7f22d2-320b-6af1-e063-6294a90addc62025-11-24WarningsExact identifier
unii: 059QF0KO0R
Pur-WashEYEWASHNiagara Pharmaceuticals, Inc.0d43b1c1-2699-37f1-e054-00144ff88e882025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.777e1559-786f-8d54-e053-2991aa0aa98d2025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.7289103a-5cbf-42f4-8848-e827149a43ca2025-11-24WarningsExact identifier
unii: 059QF0KO0R
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEAurobindo Pharma Limitedb17d54ca-5885-48d3-96e9-b29ad14f8d762025-11-24Warnings, Adverse reactionsExact identifier
rxcui: 314182
rxcui: 312515
unii: 660YQ98I10
Rain Daily Hydration and Comfort For Dry EyesGLYCERINRain Eye Drops, LLC31d7c204-fb74-fb28-e063-6294a90ab3302025-11-23WarningsExact identifier
unii: PDC6A3C0OX
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
unii: 059QF0KO0R
ECZEMANICCOLUM SULPHURICUM, KALI BROMATUM, KALI MURIATICUM, HEPAR SULPHURIS CALCAREUM, KALI BICHROMICUM, KALI SULPHURICUM, SULPHUR.PLYMOUTH HEALTHCARE PRODUCTS LLC624d8671-43ce-46a8-87d3-d491fd9ba9132025-11-20WarningsExact identifier
unii: 660YQ98I10
ColdBAPTISIA TINCTORIA, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM, LOMATIUM DISSECTUM, PUERARIA LOBATA, TRIFOLIUM PRATENSE, PHYTOLACCA DECANDRA, ALLIUM CEPA, ARSENICUM IODATUM, BARYTA CARBONICA, BROMIUM, CALCAREA CARBONICA, KALI MURIATICUM, LACHESIS MUTUS, MERCURIUS SOLUBILIS, SILICEANatural Creations, Incc45d1d8f-24be-4c13-8c4b-3889624214152025-11-20WarningsExact identifier
unii: 660YQ98I10
COLD/FLU HPARSENICTRIOXIDE,BAPTISIATINCTORIAROOT,BRYONIAALBAROOT,SOLANUMDULCAMARATOP,ECHINACEAANGUSTIFOLIA,ECHINACEAPURPUREA,EUPATORIUMPERFOLIATUMFLOWERINGTOP,FERROSOFERRICPHOSPHATE,GELSEMIUMSEMPERVIRENSROOT,POTASSIUMCHLORIDE,PHOSPHORUS,ANEMONEPULSATILLA,SULFUR,ZINCACETATEANHYDROUS,ZINCCARBONATE,ZINC,ZINCCHLORIDE,ZINCOXIDE,ZINCPICRATENONAHYRDATE,ZINCVALERATEDIHYDRATE,CAIRINAMOSCHATAHEART/LIVERAUTOLYSATE,INFLUENZINUMNatural Creations, Inc.11d945ea-3b03-42cc-b1c0-e4c517e386f62025-11-20WarningsExact identifier
unii: 660YQ98I10
Potassium chloridePOTASSIUM CHLORIDEAdvagen Pharma Ltd8000e242-fe20-4d02-8f7d-97298857cf4c2025-11-19Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

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