Digestive Relief

Product NDC: 11673-372
11-digit product format: 116730372
Labeler code: 11673
Product ID: 11673-372_ab00dcf1-79d0-4510-b957-db68ab712117
Type: HUMAN OTC DRUG
Nonproprietary name: Bismuth subsalicylate
Dosage form: LIQUID
Route: ORAL
Labeler: TARGET Corporation
Application: M008
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-07-31
Marketing end: 2026-12-28
Substance: BISMUTH SUBSALICYLATE
Active strength: 525 mg/30mL
Pharmacologic classes: Bismuth [CS], Bismuth [EPC]
NDC exclude flag: No
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 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	11673-372		D	Discontinued by firm	2026-10-12
excluded package	package	11673-372	11673-372-00	D	Discontinued by firm	2026-10-12
excluded package	package	11673-372	11673-372-32	D	Discontinued by firm	2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 38 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11673-372-32	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	11673-372-32	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	11673-372-32	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	11673-372-32	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	11673-372-32	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	11673-372-32	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	11673-372-32	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	11673-372-32	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	11673-372-32	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	11673-372-32	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	11673-372-32	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	11673-372-32	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	11673-372-32	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	11673-372-32	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	11673-372-32	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	11673-372-32	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	11673-372-32	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	11673-372-32	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	11673-372-32	`8dfbde2a14a4…`	`c9ff85d89658…`

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: Digestive Relief
Brand name suffix: Regular Strength

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BISMUTH SUBSALICYLATE	525 mg/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
62TEY51RR1	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
308762	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
90b0c541-2834-4ed7-9d01-76080dd73057	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15	Product name	1	20240313
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11673-372-32	2021-01-29	C162847	48780-1	ba0f9c33-489c-a910-e053-dadaa90a0b85	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11673-372-08	Digestive ReliefRegular Strength	236 mL in 1 BOTTLE, PLASTIC	LIQUID	236	8
11673-372-16	Digestive ReliefRegular Strength	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473	8
11673-372-32	Digestive ReliefRegular Strength	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473	1
11673-372-32	Digestive ReliefRegular Strength	2 in 1 PACKAGE	LIQUID	2	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-372	DIGESTIVE RELIEF REGULAR STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [TARGET CORPORATION]	8	Current NDC, Legacy NDC, 2 package rows	20240608_90b0c541-2834-4ed7-9d01-76080dd73057.zip
11673-372	DIGESTIVE RELIEF REGULAR STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [TARGET CORPORATION]	1	Current NDC, Legacy NDC, 2 package rows	20191108_8565a0ba-ac10-463e-8c3d-eee1204b7f1f.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 6 of 10 · 198 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	CARDINAL HEALTH 110, LLC. DBA LEADER	7d6047a9-5557-487a-ae06-f904dac626c9	2025-10-14	Warnings	Exact identifier application number: M008
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	Atlantic Biologicals Corp	401f8393-680c-e1a8-e063-6394a90a81ab	2025-10-01	Warnings	Exact identifier application number: M008
First Aid Direct Peptum Tabs	BISMUTH SUBSALICYLATE	Cintas Corp	dd14cd57-3f7c-4634-9da9-6f83dc5bae12	2025-09-29	Warnings	Exact identifier application number: M008
RIGHT REMEDIES Stomach Relief BISMUTH SUBSALICYLATE 262 mg softgel	BISMUTH SUBSALICYLATE	Strive Pharmaceuticals Inc.	0f271054-fa96-4475-8279-65f4565aba36	2025-09-22	Warnings	Exact identifier application number: M008
Bismuth Subsalicylate Suspension Regular Strength	BISMUTH SUBSALICYLATE	FSA Store Inc. (Caring Mill)	fbabc313-600a-4722-9948-1a3e21414059	2025-09-18	Warnings	Exact identifier application number: M008
QUALITY CHOICE ULTRA STRENGTH STOMACH RELIEF	BISMUTH SUBSALICYLATE	QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)	67c610b1-fe94-4ad3-ad1a-8bd93a4da9d9	2025-09-11	Warnings	Exact identifier application number: M008
Medique Diotame	BISMUTH SUBSALICYLATE	Unifirst First Aid Corporation	0667ec26-c2cd-153c-e054-00144ff88e88	2025-09-08	Warnings	Exact identifier application number: M008
McKesson Bismuth	BISMUTH SUBSALICYLATE	McKesson Medical-Surgical	d1f3dfa4-e021-6384-e053-2995a90a7b42	2025-09-08	Warnings	Exact identifier application number: M008
Medi-First Pep-T-Med	BISMUTH SUBSALICYLATE	Unifirst First Aid Corporation	88f4d5d4-92ed-40ab-97a9-181da72f869b	2025-09-08	Warnings	Exact identifier application number: M008
Thompson Chewable Bismuth Tabs	BISMUTH SUBSALICYLATE	Thompson Safety LLC	c94b9bc2-b764-a9a7-e053-2a95a90aed81	2025-09-08	Warnings	Exact identifier application number: M008
Goodsense Regular strength Stomach Relief 122	BISMUTH SUBSALICYLATE	Preferred Pharmaceuticals Inc.	f0588ab8-d1fc-419a-8d68-bee42332d50f	2025-08-01	Warnings	Exact identifier application number: M008
Ultra Strength Stomach Relief	BISMUTH SUBSALICYLATE 525 MG	Retail Business Services, LLC.	338ca589-91ff-30ed-e063-6294a90a243a	2025-07-21	Warnings	Exact identifier application number: M008
Regular Strength Stomach Relief	BISMUTH SUBSALICYLATE 525 MG	Retail Business Services, LLC.	338d61af-35a8-fba7-e063-6294a90a38e8	2025-07-21	Warnings	Exact identifier application number: M008
Senna	SENNOSIDES	Major Pharmaceuticals	cfb6bf89-c77e-4372-9bc9-44d6a659c955	2025-07-18	Warnings	Exact identifier application number: M008
Major Bismuth Subsalicylate	BISMUTH SUBSALICYLATE	Major Pharmaceuticals	2a7c9cc1-206e-4018-b89d-7b634df43df6	2025-07-11	Warnings	Exact identifier application number: M008
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	55440401-f82f-45a3-ba7e-6ccdfdacead3	2025-07-10	Warnings	Exact identifier application number: M008
Upset Stomach Relief-Bismuth Subsalicylate 262 mg	BISMUTH SUBSALICYLATE 262 MG	Pioneer Life Sciences, LLC	07e2cc82-ab0e-46c5-863b-67658b612678	2025-06-27	Warnings	Exact identifier application number: M008
Upset Stomach Relief-Bismuth Subsalicylate 262 mg	BISMUTH SUBSALICYLATE 262 MG	NUVICARE LLC	6697e464-00ac-41de-a7ea-d7bb24ed5e2a	2025-06-25	Warnings	Exact identifier application number: M008
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	P & L Development, LLC	8383945f-b3a7-4242-bfaa-acf24b66406d	2025-05-30	Warnings	Exact identifier application number: M008
5-Symptom Digestive Relief	BISMUTH SUBSALICYLATE	TARGET CORPORATION	28fba615-48ca-8d96-e063-6394a90a2797	2025-04-12	Warnings	Exact identifier application number: M008

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
62TEY51RR1	BISMUTH SUBSALICYLATE	14882-18-9	BISMUTH SUBSALICYLATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
308762	bismuth subsalicylate 525 MG in 30 mL Oral Suspension	PSN	90b0c541-2834-4ed7-9d01-76080dd73057	8
308762	bismuth subsalicylate 17.5 MG/ML Oral Suspension	SCD	90b0c541-2834-4ed7-9d01-76080dd73057	8
308762	bismuth subsalicylate 1.75 % Oral Suspension	SY	90b0c541-2834-4ed7-9d01-76080dd73057	8
308762	bismuth subsalicylate 262 MG per 15 ML Oral Suspension	SY	90b0c541-2834-4ed7-9d01-76080dd73057	8
308762	bismuth subsalicylate 524 MG per 30 ML Oral Suspension	SY	90b0c541-2834-4ed7-9d01-76080dd73057	8
308762	bismuth subsalicylate 525 MG per 30 ML Oral Suspension	SY	90b0c541-2834-4ed7-9d01-76080dd73057	8
308762	bismuth subsalicylate 525 MG in 30 mL Oral Suspension	PSN	8565a0ba-ac10-463e-8c3d-eee1204b7f1f	1
308762	bismuth subsalicylate 17.5 MG/ML Oral Suspension	SCD	8565a0ba-ac10-463e-8c3d-eee1204b7f1f	1
308762	bismuth subsalicylate 1.75 % Oral Suspension	SY	8565a0ba-ac10-463e-8c3d-eee1204b7f1f	1
308762	bismuth subsalicylate 262 MG per 15 ML Oral Suspension	SY	8565a0ba-ac10-463e-8c3d-eee1204b7f1f	1
308762	bismuth subsalicylate 524 MG per 30 ML Oral Suspension	SY	8565a0ba-ac10-463e-8c3d-eee1204b7f1f	1
308762	bismuth subsalicylate 525 MG per 30 ML Oral Suspension	SY	8565a0ba-ac10-463e-8c3d-eee1204b7f1f	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-372-08	11673037208	236 mL in 1 BOTTLE, PLASTIC (11673-372-08)	236 ml	2018-07-31	2026-12-28	No	No	Current
11673-372-16	11673037216	473 mL in 1 BOTTLE, PLASTIC (11673-372-16)	473 ml	2018-07-31	2026-12-28	No	No	Current
11673-372-32	11673037232	473 mL in 1 BOTTLE, PLASTIC	473 ml					Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	TARGET Corporation	2026-09-09	HUMAN OTC DRUG LABEL	9
Drug Facts	TARGET Corporation	2019-11-07	HUMAN OTC DRUG LABEL	1