Stomach Relief

Product NDC: 17856-1286
11-digit product format: 178561286
Labeler code: 17856
Product ID: 17856-1286_34f36bfa-3ffc-825c-e063-6394a90a45b9
Type: HUMAN OTC DRUG
Nonproprietary name: Bismuth subsalicylate
Dosage form: LIQUID
Route: ORAL
Labeler: ATLANTIC BIOLOGICALS CORP.
Application: M
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-03-29
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

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 · 9 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
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	17856-1286-1	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	17856-1286-2	`1332a3947898…`	`d4bfe170f9cd…`
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	17856-1286-2	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	17856-1286-1	`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	17856-1286-2	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	17856-1286-1	`bd6a592717d7…`	`303034d00443…`

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: Stomach 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
5c02d0ba-91e4-4bd2-ac66-6905323653b2	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, Related label table
NDC	Effective	Related label
17856-1286-1	2024-04-19	Drug Facts
17856-1286-2	2024-04-19	Drug Facts
17856-1286-1	2024-01-30	Drug Facts
17856-1286-2	2024-01-30	Drug Facts
17856-1286-1	2022-05-19	Drug Facts
17856-1286-2	2022-05-19	Drug Facts
17856-1286-1	2022-01-28	Drug Facts
17856-1286-2	2022-01-28	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
17856-1286-1	Stomach ReliefRegular Strength	50 in 1 BOX, UNIT-DOSE	LIQUID	50	5
17856-1286-2	Stomach ReliefRegular Strength	50 in 1 BOX, UNIT-DOSE	LIQUID	50	5
17856-1286-3	Stomach ReliefRegular Strength	15 mL in 1 CUP, UNIT-DOSE	LIQUID	15	5
17856-1286-4	Stomach ReliefRegular Strength	30 mL in 1 CUP, UNIT-DOSE	LIQUID	30	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17856-1286	STOMACH RELIEF REGULAR STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [ATLANTIC BIOLOGICALS CORP.]	5	Current NDC, Legacy NDC, 4 package rows	20250514_5c02d0ba-91e4-4bd2-ac66-6905323653b2.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 6 · 111 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MAX relief junior	ACETAMINOPHEN	ATLANTIC BIOLOGICALS CORP.	396903dc-ae2d-4bf4-b1fd-0017b84abef9	2024-02-28	Warnings	Exact identifier application number: M
MAX relief junior	ACETAMINOPHEN	ATLANTIC BIOLOGICALS CORP.	44730cbd-5b98-49bd-b3b8-6fecb0ccd153	2024-02-28	Warnings	Exact identifier application number: M
HYDROCORTISONE	HYDROCORTISONE ACETATE	HART Health	779f945f-ab69-40de-8d86-ab76debc5c7c	2024-02-16	Warnings	Exact identifier application number: M
First Aid and Burn	BENZALKONIUM CHLORIDE, LIDOCAINE	HART Health	f5746bba-9d7f-4691-b466-14985473bf14	2024-02-16	Warnings	Exact identifier application number: M
IBUPROFEN	IBUPROFEN	HART Health	1c1374e1-890f-48ab-8f93-e84da9d5bf84	2024-01-25	Warnings	Exact identifier application number: M
Hand Sanitizer	ANTISEPTIC GEL	HART Health	f07daf29-d0db-4cf8-8baf-d175c2b2ef50	2024-01-25	Warnings	Exact identifier application number: M
Hydrogen Peroxide	HYDROGEN PEROXIDE	HART Health	0346a322-8f6e-405a-8d17-8bc6ce5105a3	2024-01-24	Warnings	Exact identifier application number: M
Alcohol	ISOPROPYL ALCOHOL	NorMed	441b915a-287f-4734-b4d9-730b3d95e04c	2024-01-24	Warnings	Exact identifier application number: M
Sooth-a-Sting	BENZOCAINE	HART Health	bd7229b6-813a-4149-bfe2-fe682f270ff4	2024-01-18	Warnings	Exact identifier application number: M
First Aid	BENZALKONIUM CHLORIDE, BENZOCAINE	HART Health	a6d258ed-6d6d-42f0-9994-6c2c4c3d0f4a	2024-01-18	Warnings	Exact identifier application number: M
TRIBIOTIC	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	HART Health	d8f175f9-f526-4c73-a171-49309ca16cb0	2024-01-18	Warnings, Adverse reactions	Exact identifier application number: M

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	5c02d0ba-91e4-4bd2-ac66-6905323653b2	5
308762	bismuth subsalicylate 17.5 MG/ML Oral Suspension	SCD	5c02d0ba-91e4-4bd2-ac66-6905323653b2	5
308762	bismuth subsalicylate 1.75 % Oral Suspension	SY	5c02d0ba-91e4-4bd2-ac66-6905323653b2	5
308762	bismuth subsalicylate 262 MG per 15 ML Oral Suspension	SY	5c02d0ba-91e4-4bd2-ac66-6905323653b2	5
308762	bismuth subsalicylate 524 MG per 30 ML Oral Suspension	SY	5c02d0ba-91e4-4bd2-ac66-6905323653b2	5
308762	bismuth subsalicylate 525 MG per 30 ML Oral Suspension	SY	5c02d0ba-91e4-4bd2-ac66-6905323653b2	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
17856-1286-1	17856128601	50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1286-1) / 15 mL in 1 CUP, UNIT-DOSE (17856-1286-3)		2024-04-18	0000-00-00	No	No	Current
17856-1286-2	17856128602	50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1286-2) / 30 mL in 1 CUP, UNIT-DOSE (17856-1286-4)		2024-04-18	0000-00-00	No	No	Current
17856-1286-3	17856128603	15 mL in 1 CUP, UNIT-DOSE	15 ml					Historical
17856-1286-4	17856128604	30 mL in 1 CUP, UNIT-DOSE	30 ml					Historical