Digestive Relief

Product NDC: 11673-372
11-digit product format: 116730372
Labeler code: 11673
Product ID: 11673-372_d7081994-555a-499a-b519-36f99f97edb8
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
Substance: BISMUTH SUBSALICYLATE
Active strength: 525 mg/30mL
Pharmacologic classes: Bismuth [CS], Bismuth [EPC]
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	11673-372		I	Inactivated by FDA		2026-08-17
excluded package	package	11673-372	11673-372-32	I	Inactivated by FDA		2026-08-17

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…`

Additional Listing Data#

Finished product: Yes
Brand name base: Digestive Relief
Brand name suffix: Regular Strength
Listing expiration: 2026-12-31

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 1 of 12 · 228 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Health Stomach relief Cherry Flavor	BISMUTH SUBSALICYLATE	CVS PHARMACY,INC.	c0bb2b6e-8187-495e-8eac-2324fae86cf5	2026-08-13	Warnings	Exact identifier application number: M008
CVS Stomach Relief	BISMUTH SUBSALICYLATE	CVS	eb96b2bb-7b2a-4664-96ac-73c917c84c30	2026-08-13	Warnings	Exact identifier application number: M008
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	Care One (Retail Business Services, LLC.)	1af2a7dd-45d7-41a0-af61-4a588f1c1985	2026-08-12	Warnings	Exact identifier application number: M008
WinCo FOODS Ultra Strength Stomach Relief	BISMUTH SUBSALICYLATE	WINCO FOODS	acf82012-0e40-4d50-b1f1-f36dc3dfad84	2026-08-07	Warnings	Exact identifier application number: M008
WinCo FOODS Stomach Relief	BISMUTH SUBSALICYLATE	WINCO FOODS	19c14efc-bf5f-4ef5-a727-aaccfae093f0	2026-08-07	Warnings	Exact identifier application number: M008
WinCo FOODS Stomach Relief	BISMUTH SUBSALICYLATE	WINCO FOODS LLC	53ae695d-f812-462d-9487-8fb5db0aa27d	2026-08-07	Warnings	Exact identifier application number: M008
nexmed multi symptom stomach relief	BISMUTH SUBSALICYLATE 262 MG	Shield Pharmaceuticals Corp	212ccf1f-faaf-4f77-9722-28713fc42761	2026-08-05	Warnings	Exact identifier application number: M008
nexmed multi symptom stomach relief	BISMUTH SUBSALICYLATE 262 MG	Shield Pharmaceuticals Corp	7c0ca713-643a-46bd-9d9a-21ac39c808c4	2026-08-05	Warnings	Exact identifier application number: M008
Stomach Relief	BISMUTH SUBSALICYLATE	Shield Pharmaceuticals Corp	8177318d-427b-4bfc-9d7f-51d1545f4eb8	2026-07-27	Warnings	Exact identifier application number: M008
Pepto Bismol Chews	BISMUTH SUBSALICYLATE	The Procter & Gamble Manufacturing Company	bb8d2ed8-54a2-2295-e053-2995a90a10ac	2026-07-27	Warnings	Exact identifier application number: M008
Pepto Bismol Chews	BISMUTH SUBSALICYLATE	The Procter & Gamble Manufacturing Company	cfe9214d-25e9-7729-e053-2a95a90a0dfb	2026-07-27	Warnings	Exact identifier application number: M008
Pepto Bismol	BISMUTH SUBSALICYLATE	The Procter & Gamble Manufacturing Company	252b143f-eee8-f407-e063-6394a90a0a08	2026-07-27	Warnings	Exact identifier application number: M008
FEVIA Diarrhea Control	BISMUTH SUBSALICYLATE	VIVUNT PHARMA LLC	4b20f189-e979-8198-e063-6294a90a7169	2026-07-16	Warnings	Exact identifier application number: M008
FEVIA Diarrhea Control	BISMUTH SUBSALICYLATE	VIVUNT PHARMA LLC	4bd5aa23-37aa-b818-e063-6394a90ae06c	2026-07-15	Warnings	Exact identifier application number: M008
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)	d20af4fb-d579-4d1e-86ae-342933f4de75	2026-07-15	Warnings	Exact identifier application number: M008
Stomach Relief	BISMUTH SUBSALICYLATE	WALMART INC. (see also Equate)	369fe912-dd0e-4ff3-a597-5ee81332838a	2026-07-15	Warnings	Exact identifier application number: M008
Stomach Relief Ultra	BISMUTH SUBSALICYLATE	EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)	642c14bd-be99-410b-9ba7-6e71c9705230	2026-07-15	Warnings	Exact identifier application number: M008
Good Neighbor Ultra Strength Stomach Relief	BISMUTH SUBSALICYLATE	AMERISOURCE BERGEN	71c30b10-db24-4a42-a4f4-db552e3d5fe6	2026-07-13	Warnings	Exact identifier application number: M008
Pepto Bismol CHEWABLES	BISMUTH SUBSALICYLATE	Select Consumer Group	5611c6cb-5c0b-cf4e-e063-6394a90abff8	2026-07-07	Warnings	Exact identifier application number: M008
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	Rugby Laboratories	6166c04e-20c6-4678-b16d-517474445698	2026-06-26	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	0000-00-00	No	No	Current
11673-372-16	11673037216	473 mL in 1 BOTTLE, PLASTIC (11673-372-16)	473 ml	2018-07-31	2022-12-30	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	2024-06-06	HUMAN OTC DRUG LABEL	8
Drug Facts	TARGET Corporation	2019-11-07	HUMAN OTC DRUG LABEL	1