NDC 81033-412-30 - 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
81033-412
Requested NDC
81033-412-30
Package NDCs from labels
81033-412-15, 81033-412-51, 81033-412-50, 81033-412-30, 81033-412-32, 81033-412-34
Manufacturer
Kesin Pharma
Effective date
2024-12-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Potassium Chloride - Kesin PharmaKesin Pharma2024-12-04HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81033-412-15Potassium Chloride15 mL in 1 CUP, UNIT-DOSESOLUTION155
81033-412-30Potassium Chloride30 mL in 1 CUP, UNIT-DOSESOLUTION305
81033-412-32Potassium Chloride100 in 1 CASESOLUTION1005
81033-412-34Potassium Chloride50 in 1 CASESOLUTION505
81033-412-50Potassium Chloride100 in 1 CASESOLUTION1005
81033-412-51Potassium Chloride50 in 1 CASESOLUTION505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81033-412POTASSIUM CHLORIDE SOLUTION [KESIN PHARMA]56 package rows20241207_17fa41e8-1918-1b88-e063-6394a90ade3f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
81033-412-15ML - Milliliter81033-412bbfbf218-c6fa-4f1f-a0b0-fd6c4857713512024-08-12
81033-412-30ML - Milliliter81033-412b5400981-8240-485c-9d9f-87593850377e12024-08-12
81033-412-32ML - Milliliter81033-4121d5cbd7d-98e5-4435-a285-be3bbff8b14a12024-08-12
81033-412-34ML - Milliliter81033-412ee33d2e1-7700-4f90-a7b5-9808c406891d12024-09-09
81033-412-50ML - Milliliter81033-4123ec55d88-9e5c-430c-a4e9-fd74b75400de12024-08-12
81033-412-51ML - Milliliter81033-412a4c9fc82-8b5d-4db7-8def-ac8c2c3d5a4412024-08-12

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 32 of 55 · 1,099 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Potassium ChloridePOTASSIUM CHLORIDEAphena Pharma Solutions - Tennessee, LLC81a53ecd-2612-4efe-9491-415fff3f86e52025-01-09Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
STERILE WATERSTERILE WATERHF Acquisition Co. LLC, DBA HealthFirst74ed2a6f-824c-a1ff-e053-2a91aa0a57c02025-01-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
STERILE WATERSTERILE WATERHF Acquisition Co LLC, DBA HealthFirst77bd3c0f-f4ab-7cfa-e053-2a91aa0a1b832025-01-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
STERILE WATERSTERILE WATERHF Acquisition Co LLC, DBA HealthFirst7610bf80-61b7-982f-e053-2a91aa0ac1bb2025-01-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
N-15ECHINACEA ANGUSTIFOLIA, BAPTISIA TINCTORIA, POTASSIUM CHLORIDE, CALCIUM SULFIDE, FERROUS IODIDE, SULFUR IODIDE, AND BOS TAURUS THYMUSDNA Labs, Inc.fbcefa48-587a-43e1-b9c2-4afaef99f14a2025-01-09WarningsExact identifier
unii: 660YQ98I10
N-16MGO ENERGIZERDNA Labs, Inc.8292b900-86c1-47ea-81da-b587439c76642025-01-09WarningsExact identifier
unii: 660YQ98I10
N-24METABOLINDNA Labs, Inc.559fca2b-1093-4bdf-be70-c453f87002c32025-01-09WarningsExact identifier
unii: 660YQ98I10
T-27WATERDNA Labs, Inc.f0e9afd7-64a4-4b85-9c5f-4bf07ba4b4812025-01-09WarningsExact identifier
unii: 059QF0KO0R
Hemorrhoidal Cream with AloeGLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUMChain Drug Marketing Association2b33c710-ac17-20f9-e063-6294a90ad29c2025-01-08WarningsExact identifier
unii: PDC6A3C0OX
ANTIBACTERIAL DREAMY FLORALSGLYCERINQuimicas Handal de Centroamerica SA de CV09f73bec-516d-90f0-e063-6394a90aecab2025-01-08WarningsExact identifier
unii: PDC6A3C0OX
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEHF Acquisition Co LLC, DBA HealthFirst9508355e-e1ed-412b-e053-2a95a90aac8e2025-01-08Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEHF Acquisition Co LLC, DBA HealthFirst951ffdc3-d54f-d5e1-e053-2a95a90a79e62025-01-08Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Sterile WaterSTERILE WATER FOR INJECTIONMedefil, Inc.99e99a50-82d5-aff6-e053-2a95a90a8c562025-01-08Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
BACTERIOSTATIC WATERBACTERIOSTATIC WATERHF Acquisition Co LLC, DBA HealthFirst99b0ef9b-600a-40dc-e053-2a95a90aa07e2025-01-08Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
STERILE WATERSTERILE WATERHF Acquisition Co LLC, DBA HealthFirst99b1cb12-0b2d-0c0f-e053-2a95a90ac3b62025-01-08Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Emetrol Powder Non-DrowsySODIUM CITRATE DIHYDRATEWellSpring Pharmaceutical Corporation9d8d2ee7-9db7-4be7-8c73-511eb2e324592025-01-08WarningsExact identifier
unii: B22547B95K
Mucus-Clear Jr. NighttimeCHAMOMILLA, CINA, KALI BIC, KALI CARB, KALI MUR, PULSATILLASilver Star Brands830e4796-5371-f681-e053-2991aa0a8e832025-01-01WarningsExact identifier
unii: 660YQ98I10
Mucus Clear Allergy ReliefALLIU CEPA, CALC PHOS, EUPHRASIA, IGNATIA, KALI MUR, NAT MUR, NUX VOM, PULSATILLA, SILICASilver Star Brandsf49bdcc1-1939-6dc2-e053-2995a90a0a3b2025-01-01WarningsExact identifier
unii: 660YQ98I10
Mucus-Clear NighttimeHEPAR SULPH, KALI BIC, KALI CARB, KALI MUR, NUX VOMSilver Star Brands826c01f3-a8b6-48c7-e053-2a91aa0a3ce12025-01-01WarningsExact identifier
unii: 660YQ98I10
Mucus Clear Cough and Cold ReliefARG MET, ARSENICUM ALB, BAPTISIA, BRYPNIA, CAUSTICUM, DULCAMARA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURP, KALI BIC, KALI MUR, MERC CORROS, PHOS, PULSATILLA NUTT, SENEGA, ZINC PIC, ZINC VAL.Silver Star Brandsf4378d84-73d5-2170-e053-2a95a90a41c62025-01-01WarningsExact identifier
unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

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