E-Z-HD

Product NDC: 32909-764
11-digit product format: 329090764
Labeler code: 32909
Product ID: 32909-764_c0b3cf2c-8b69-4c19-b436-41410d638424
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: barium sulfate
Dosage form: POWDER, FOR SUSPENSION
Route: ORAL
Labeler: E-Z-EM Canada Inc
Application: NDA208036
Marketing category: NDA
Marketing start: 2016-01-11
Substance: BARIUM SULFATE
Active strength: 980 mg/g
Pharmacologic classes: Radiographic Contrast Agent [EPC], X-Ray Contrast Activity [MoA]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	RLD / RS	Approval date
N208036-001	E-Z-HD	BARIUM SULFATE	98%	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11
N208036-002	E-Z-PAQUE	BARIUM SULFATE	96%	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07
N208036-003	E-Z-CAT DRY	BARIUM SULFATE	40%	FOR SUSPENSION / ORAL	RLD	2017-01-03
N208036-004	VARIBAR THIN LIQUID	BARIUM SULFATE	81%	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 5 · 172 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-09-14 22:38:34	2026-08	N208036-001	E-Z-HD	98%	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N208036-002	E-Z-PAQUE	96%	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N208036-003	E-Z-CAT DRY	40%	FOR SUSPENSION / ORAL	RLD	2017-01-03	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N208036-004	VARIBAR THIN LIQUID	81%	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N208036-001	E-Z-HD	98%	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N208036-002	E-Z-PAQUE	96%	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N208036-003	E-Z-CAT DRY	40%	FOR SUSPENSION / ORAL	RLD	2017-01-03	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N208036-004	VARIBAR THIN LIQUID	81%	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N208036-001	E-Z-HD	98%	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N208036-002	E-Z-PAQUE	96%	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N208036-003	E-Z-CAT DRY	40%	FOR SUSPENSION / ORAL	RLD	2017-01-03	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N208036-004	VARIBAR THIN LIQUID	81%	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N208036-001	E-Z-HD	98%	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N208036-002	E-Z-PAQUE	96%	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N208036-003	E-Z-CAT DRY	40%	FOR SUSPENSION / ORAL	RLD	2017-01-03	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N208036-004	VARIBAR THIN LIQUID	81%	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N208036-001	E-Z-HD	98% (334GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N208036-002	E-Z-PAQUE	96% (169GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N208036-003	E-Z-CAT DRY	40% (9GM/POUCH)	FOR SUSPENSION / ORAL	RLD	2017-01-03	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N208036-004	VARIBAR THIN LIQUID	81% (120GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N208036-001	E-Z-HD	98% (334GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N208036-002	E-Z-PAQUE	96% (169GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N208036-003	E-Z-CAT DRY	40% (9GM/POUCH)	FOR SUSPENSION / ORAL	RLD	2017-01-03	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N208036-004	VARIBAR THIN LIQUID	81% (120GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N208036-001	E-Z-HD	98% (334GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N208036-002	E-Z-PAQUE	96% (169GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N208036-003	E-Z-CAT DRY	40% (9GM/POUCH)	FOR SUSPENSION / ORAL	RLD	2017-01-03	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N208036-004	VARIBAR THIN LIQUID	81% (120GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N208036-001	E-Z-HD	98% (334GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N208036-002	E-Z-PAQUE	96% (169GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N208036-003	E-Z-CAT DRY	40% (9GM/POUCH)	FOR SUSPENSION / ORAL	RLD	2017-01-03	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N208036-004	VARIBAR THIN LIQUID	81% (120GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N208036-001	E-Z-HD	98% (334GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N208036-002	E-Z-PAQUE	96% (169GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N208036-003	E-Z-CAT DRY	40% (9GM/POUCH)	FOR SUSPENSION / ORAL	RLD	2017-01-03	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N208036-004	VARIBAR THIN LIQUID	81% (120GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N208036-001	E-Z-HD	98% (334GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2016-01-11	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N208036-002	E-Z-PAQUE	96% (169GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2017-04-07	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N208036-003	E-Z-CAT DRY	40% (9GM/POUCH)	FOR SUSPENSION / ORAL	RLD	2017-01-03	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N208036-004	VARIBAR THIN LIQUID	81% (120GM/BOT)	FOR SUSPENSION / ORAL	RLD, RS	2019-04-30	`5bbf6a4d5a75…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: E-Z-HD
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BARIUM SULFATE	980 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
25BB7EKE2E	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
a4330804-7179-472a-91cb-84bbd5079bb8	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5dbf91a8-ec29-4ffc-807c-e3bae7fb67b1	Product name	1	20201123
85bed648-23ca-4804-98e6-e36aee999cad	Product name	1	20190717
80de93b4-8a94-428d-beb7-d644353ee70b	Product name	1	20180424
eb4f7d5b-1286-40dc-b8bf-ad87ff51c688	Product name	1	20170522
db8eb201-78c7-4590-8a71-fac0a539bd8c	Product name	1	20170404
141092be-5eb5-452e-9f69-2d350aa70a87	Product name	1	20161208

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
32909-764-01	E-Z-HD	24 in 1 CARTON	POWDER, FOR SUSPENSION	24		8
32909-764-01	E-Z-HD	340 g in 1 BOTTLE	POWDER, FOR SUSPENSION	340		8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
32909-764-01	EA - Each	32909-764	eaa47ac8-7e2d-48f2-8b57-12d05b98f4ee	2	2021-02-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Barium Sulfate	ACTIVE INGREDIENT	25BB7EKE2E	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
Barium Sulfate	ACTIVE MOIETY	25BB7EKE2E	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
acacia	INACTIVE INGREDIENT	5C5403N26O	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
anhydrous citric acid	INACTIVE INGREDIENT	XF417D3PSL	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
carrageenan sodium	INACTIVE INGREDIENT	7CY8BVL34N	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
dimethicone 1000	INACTIVE INGREDIENT	MCU2324216	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
ethyl maltol	INACTIVE INGREDIENT	L6Q8K29L05	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
polysorbate 80	INACTIVE INGREDIENT	6OZP39ZG8H	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
saccharin sodium	INACTIVE INGREDIENT	SB8ZUX40TY	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
sorbitol	INACTIVE INGREDIENT	506T60A25R	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3
trisodium citrate dihydrate	INACTIVE INGREDIENT	B22547B95K	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
32909-764	E-Z-HD (BARIUM SULFATE) POWDER, FOR SUSPENSION [E-Z-EM CANADA INC]	7	Current NDC, Legacy NDC, 2 package rows	20221108_a4330804-7179-472a-91cb-84bbd5079bb8.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 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
E-Z-Paque	BARIUM SULFATE	E-Z-EM Canada Inc	7225868a-4037-c96a-44e3-3326d36cbedc	2026-04-15	Warnings, Adverse reactions	Exact identifier application applno (NDA): 208036 application number: NDA208036
Varibar Thin Liquid	BARIUM SULFATE	E-Z-EM Canada Inc	59493c83-3941-cc84-cc37-a8696ae42873	2026-04-15	Warnings, Adverse reactions	Exact identifier application applno (NDA): 208036 application number: NDA208036
E-Z-HD	BARIUM SULFATE	E-Z-EM Canada Inc	a4330804-7179-472a-91cb-84bbd5079bb8	2026-04-15	Warnings, Adverse reactions	Exact identifier application applno (NDA): 208036 application number: NDA208036 ndc (product): 32909-764

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
25BB7EKE2E	BARIUM SULFATE	7727-43-7	BARIUM SULFATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
32909-764-01	32909076401	24 BOTTLE in 1 CARTON (32909-764-01) / 340 g in 1 BOTTLE	24 bottle	2016-04-18	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
E-Z-HD	E-Z-EM Canada Inc \| BRACCO DIAGNOSTICS INC \| CIMBAR PERFORMANCE MINERALS, INC.	2026-04-15	HUMAN PRESCRIPTION DRUG LABEL	8