FDA.reportPublic FDA data

NDC 71719-2040 - Vizumax ENEM

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
71719-2040
Package NDCs from labels
71719-2040-1, 71719-2040-2
Manufacturer
Vizumax Diagnostics LLC
Effective date
2021-10-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Vizumax ENEM - Vizumax Diagnostics LLCVizumax Diagnostics LLC2021-10-04HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
71719-2040-12022-07-29These highlights do not include all the information needed to use, see full prescribing information for additional details. Initial U.S. Approval.
71719-2040-22022-07-29These highlights do not include all the information needed to use, see full prescribing information for additional details. Initial U.S. Approval.
71719-2040-12021-10-04These highlights do not include all the information needed to use, see full prescribing information for additional details. Initial U.S. Approval.
71719-2040-22021-10-04These highlights do not include all the information needed to use, see full prescribing information for additional details. Initial U.S. Approval.
71719-2040-12021-01-29These highlights do not include all the information needed to use, see full prescribing information for additional details. Initial U.S. Approval.
71719-2040-22021-01-29These highlights do not include all the information needed to use, see full prescribing information for additional details. Initial U.S. Approval.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71719-2040-1Vizumax ENEM454 g in 1 BAGPOWDER, FOR SUSPENSION4544
71719-2040-2Vizumax ENEM397 g in 1 BAGPOWDER, FOR SUSPENSION3974

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71719-2040VIZUMAX ENEM (BARIUM SULFATE) POWDER, FOR SUSPENSION [VIZUMAX DIAGNOSTICS LLC]42 package rows20211005_2a9517f0-533c-4a22-88ab-e0aa5fd57b4d.zip

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 1 of 8 · 145 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TheraTearsCARBOXYMETHYLCELLULOSE SODIUMMEDTECH PRODUCTS INC17a01236-130f-495b-9f8d-92b6a23b2dc52026-09-09WarningsExact identifier
unii: K679OBS311
REFRESH LIQUIGELCARBOXYMETHYLCELLULOSE SODIUMAllergan, Inc.4b8b2f6a-4b89-446c-9e5b-9b83c453a01d2026-08-28WarningsExact identifier
unii: K679OBS311
Droptics Dry Eye ReliefCARBOXYMETHYLCELLULOSE SODIUM,GLYCERIN,POLYSORBATE 80Droptics LLC29d7614b-f4b7-48e2-97c5-d1bff27731d22026-07-22WarningsExact identifier
unii: K679OBS311
Retaine CMCCARBOXYMETHYLCELLULOSE SODIUMOCuSOFT LLCa3698c71-0c80-4246-be52-5e7d96f6c5402026-07-06WarningsExact identifier
unii: K679OBS311
Leukotrap WB SystemCPDA-1 BLOOD BAG COLLECTION SYSTEMGVS TM INC54fd8a72-0527-df0c-e063-6294a90abe752026-06-24Exact identifier
unii: 1Q73Q2JULR
Leukotrap WB SystemCPDA-1 BLOOD BAG COLLECTION SYSTEMGVS TM INC54fddca1-b40c-7af0-e063-6294a90a410e2026-06-24Exact identifier
unii: 1Q73Q2JULR
Leukotrap WB SystemCPDA-1 BLOOD BAG COLLECTION SYSTEMGVS TM INC54fdf83e-f641-1f69-e063-6394a90ab7502026-06-24Exact identifier
unii: 1Q73Q2JULR
Lubricant EyeCARBOXYMETHYLCELLULOSE SODIUM 0.5%CARDINAL HEALTH 110, LLC. DBA LEADER51a2d74f-5ff3-9921-e063-6294a90a345a2026-06-15WarningsExact identifier
unii: K679OBS311
Lubricant EyeCARBOXYMETHYLCELLULOSE SODIUMRugby Laboratories51cadca6-a31b-c1b5-e063-6394a90a34d32026-06-15WarningsExact identifier
unii: K679OBS311
Sodium Citrate and Citric AcidSODIUM CITRATE AND CITRIC ACID MONOHYDRATECardinal Health 107, LLCb3d5225c-0ee4-481e-b9ec-bc5e1321096d2026-06-12Adverse reactionsExact identifier
unii: 1Q73Q2JULR
REFRESH CELLUVISCCARBOXYMETHYLCELLULOSE SODIUMAllergan, Inc.b32ed9e8-d091-4f16-b416-5a62cdfee49a2026-06-05WarningsExact identifier
unii: K679OBS311
C-More Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUM, GLYCERINPROFOUND NUTRITION LIMITED78f04ecb-da5e-468c-81fe-70f7c26b76c22026-06-01WarningsExact identifier
unii: K679OBS311
Varibar Thin HoneyBARIUM SULFATEE-Z-EM Canada Inc37bf7f08-5486-e570-7f80-0e0ee5cd33e82026-05-15Warnings, Adverse reactionsExact identifier
unii: 25BB7EKE2E
Varibar PuddingBARIUM SULFATEE-Z-EM Canada Inc553285e2-d0e9-8b7b-4766-a0a6b9496f872026-05-15Warnings, Adverse reactionsExact identifier
unii: 25BB7EKE2E
Varibar NectarBARIUM SULFATEE-Z-EM Canada Inc5e7045f7-b771-d8af-ce30-be95b2597c102026-05-15Warnings, Adverse reactionsExact identifier
unii: 25BB7EKE2E
ENTERO Vu 24%BARIUM SULFATEE-Z-EM Canada Inc83a06a8e-93db-a59b-933c-5882127bce7c2026-05-15Warnings, Adverse reactionsExact identifier
unii: 25BB7EKE2E
REFRESH TEARS PFCARBOXYMETHYLCELLULOSE SODIUM, GLYCERINAllergan, Inc.9e1cba7b-84ed-47f3-b19a-1219928343502026-04-24WarningsExact identifier
unii: K679OBS311
MannitolMANNITOLHospira, Inc.8ad3145e-00e7-4412-b9a5-06f00f264f302026-04-21Warnings, Adverse reactionsExact identifier
unii: 3OWL53L36A
E-Z-PaqueBARIUM SULFATEE-Z-EM Canada Inc7225868a-4037-c96a-44e3-3326d36cbedc2026-04-15Warnings, Adverse reactionsExact identifier
unii: 25BB7EKE2E
E-Z-PaqueBARIUM SULFATEE-Z-EM Canada Inc2ecea1ab-66c8-4eb0-8503-6d6b41b513282026-04-15Warnings, Adverse reactionsExact identifier
unii: 25BB7EKE2E

Reported adverse events (FAERS/openFDA)#

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