FDA.reportPublic FDA data

E-Z-Paste

Product NDC
32909-770
Requested package NDC
32909-770-01
11-digit product format
329090770
Labeler code
32909
Product ID
32909-770_9bec29c9-b479-cbd9-6d0c-42de42dee2f0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Barium Sulfate
Dosage form
CREAM
Route
ORAL
Labeler
E-Z-EM Canada Inc
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
1974-06-01
Substance
BARIUM SULFATE
Active strength
.6 g/g
Pharmacologic classes
Radiographic Contrast Agent [EPC], X-Ray Contrast Activity [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage32909-77032909-770-01DDiscontinued by firm2026-08-11

Additional Listing Data#

Finished product
Yes
Brand name base
E-Z-Paste
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BARIUM SULFATE.6 g/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
25BB7EKE2EInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
704132ea-4986-0b2c-2dd4-de89c0282a15Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5dbf91a8-ec29-4ffc-807c-e3bae7fb67b1Product name120201123
85bed648-23ca-4804-98e6-e36aee999cadProduct name120190717
80de93b4-8a94-428d-beb7-d644353ee70bProduct name120180424
eb4f7d5b-1286-40dc-b8bf-ad87ff51c688Product name120170522
db8eb201-78c7-4590-8a71-fac0a539bd8cProduct name120170404
141092be-5eb5-452e-9f69-2d350aa70a87Product name120161208

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
32909-770-01E-Z-Paste1 in 1 BOXCREAM14
32909-770-01E-Z-Paste454 g in 1 TUBECREAM4544

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
32909-770-01GM - Gram32909-77046783b40-71cc-46e1-aba8-0271faa1cdd412014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BARIUM SULFATEACTIVE INGREDIENT25BB7EKE2EE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
BARIUM SULFATEACTIVE MOIETY25BB7EKE2EE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
CARBOXYMETHYLCELLULOSE SODIUMINACTIVE INGREDIENTK679OBS311E-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
DIMETHICONE 1000INACTIVE INGREDIENTMCU2324216E-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
DIMETHICONE 350INACTIVE INGREDIENT2Y53S6ATLUE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
ETHYL VANILLININACTIVE INGREDIENTYC9ST449YJE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9TE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OHE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
SACCHARIN SODIUMINACTIVE INGREDIENTSB8ZUX40TYE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4E-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
SORBITOLINACTIVE INGREDIENT506T60A25RE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
TRISODIUM CITRATE DIHYDRATEINACTIVE INGREDIENTB22547B95KE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1
WATERINACTIVE INGREDIENT059QF0KO0RE-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
32909-770E-Z-PASTE (BARIUM SULFATE) CREAM [E-Z-EM CANADA INC]3Current NDC, Legacy NDC, 2 package rows20230802_704132ea-4986-0b2c-2dd4-de89c0282a15.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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
E-Z-PasteBARIUM SULFATEE-Z-EM Canada Inc704132ea-4986-0b2c-2dd4-de89c0282a152025-12-18Warnings, Adverse reactionsExact identifier
ndc (package): 32909-770-01
ndc (product): 32909-770
ndc11 (package): 32909077001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
32909-770-01329090770011 TUBE in 1 BOX (32909-770-01) > 454 g in 1 TUBE1 tube1974-06-010000-00-00NoNoCurrent