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 10 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	P & L Development, LLC	7a461b91-d11f-4cb9-be61-c7d91d278302	2024-04-16	Warnings	Exact identifier application number: M008
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	Gobrands, Inc. (Goodnow)	cd647eb7-6e03-415c-8249-89c126824d00	2024-04-03	Warnings	Exact identifier application number: M008
Stomach Relief Ultra Strength	BISMUTH SUBSALICYLATE	Care One (Retail Business Services, LLC.)	c443b640-18b0-4b7d-a13c-0accb915a801	2024-03-05	Warnings	Exact identifier application number: M008
Stomach Relief - Regular Strength	BISMUTH SUBSALICYLATE	AptaPharma Inc.	970b4118-2c2e-4806-8fe8-937ba06cf6e9	2023-12-30	Warnings	Exact identifier application number: M008
Stomach Relief, Maximum Strength	BISMUTH SUBSALICYLATE	AptaPharma Inc.	cdd436f6-b769-49aa-9e6c-da512da9e6e3	2023-12-30	Warnings	Exact identifier application number: M008
Stomach Relief - Maximum Strength	BISMUTH SUBSALICYLATE	AptaPharma Inc.	15cd9163-16d6-4332-9e26-77c05e0a26a7	2023-12-30	Warnings	Exact identifier application number: M008
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	Demoulas Super Markets Inc	9a95d198-f3ba-4bc3-a6f1-e065eb7e86f0	2023-12-29	Warnings	Exact identifier application number: M008
Stomach Relief Maximum Strength	BISMUTH SUBSALICYLATE	Demoulas Super Markets Inc	b2d55045-d4a4-4167-a20c-42932f35bab2	2023-12-29	Warnings	Exact identifier application number: M008
STOMACH RELIEF	BISMUTH SUBSALICYLATE	Consumer Value Products, Inc.	7526a3f2-ce7c-46c8-8ddf-1bcaf313876d	2023-12-29	Warnings	Exact identifier application number: M008
Estomaquil Polvo	BISMUTH SUBSALICYLATE	ProMex LLC	cf94c99a-c489-45ec-bb13-3e6959e377de	2023-11-29	Warnings	Exact identifier application number: M008
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	Care One (Retail Business Services, LLC.)	3c53adaa-275f-4164-b21e-285e4f03433e	2023-10-05	Warnings	Exact identifier application number: M008
Pepto-Bismol Chewable, TRAVEL BASIX	BISMUTH SUBSALICYLATE	Lil' Drug Store Products, Inc.	dd2f2205-34d1-4960-bf37-bb8d534cd0e1	2023-10-03	Warnings	Exact identifier application number: M008
Stomach Relief	BISMUTH SUBSALICYLATE	CDMA- QC	fe3cd0ce-933b-4ad3-a34f-c057a9356158	2021-06-16	Warnings	Exact identifier application number: M008
Topcare Stomach Relief Original Strength	BISMUTH SUBSALICYLATE	TopCo Associates, LLC	e4b1929c-0967-44ea-8552-6549aa2a464e	2018-12-14	Warnings	Exact identifier application number: M008
Bismuth	BISMUTH SUBSALICYLATE	Allegiant Health	015ca07a-f6b5-4741-a7b0-821cf6d4e418	2018-11-07	Warnings	Exact identifier application number: M008
Gastrobiz	BISMUTH SUBSALICYLATE	Allegiant Health	aa516512-afd7-453f-9c73-5fa930cafac3	2018-09-11	Warnings	Exact identifier application number: M008
Pep Tum	BISMUTH SUBSALICYLATE	First Aid Direct	bf966e9f-2f95-41cd-a6e5-b8eb521181d8	2017-12-22	Warnings	Exact identifier application number: M008
Bismuth Chewable	BISMUTH SUBSALICYLATE 262 MG	Marc Glassman, Inc.	cdfcfdc2-ed5e-49d8-b16f-e32748d82e3e	2016-12-19	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