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…`

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 1 of 6 · 111 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MG DermaSpray 70	ETHYL ALCOHOL	Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.	153ed8ff-5632-4f21-84de-2b87ac2bef31	2026-08-04	Warnings	Exact identifier application number: M
The Original Mane n Tail Daily Control 2 in 1 Anti Dandruff	PYRITHIONE ZINC	Straight Arrow Products Inc	68ab55d6-b1a9-46c0-87f0-ec12ad3474bc	2026-07-09	Warnings	Exact identifier application number: M
Stool Softener Laxative	DOCUSATE SODIUM	ATLANTIC BIOLOGICALS CORP.	c1f588d0-4600-4b97-b2d3-2c08ac351e07	2026-06-30	Warnings	Exact identifier application number: M
Docusate Sodium	DOCUSATE SODIUM	PD-Rx Pharmaceuticals, Inc.	66ca7a94-378b-4476-8060-d9c6f82f57fc	2026-06-12	Warnings	Exact identifier application number: M
TRIBIOTIC	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	HART Health	3d17aba0-220f-42c4-9e26-5c44857847cd	2026-05-20	Warnings, Adverse reactions	Exact identifier application number: M
IT Cosmetics Your Skin But Better CC Plus Color Correcting Broad Spectrum SPF 50 Plus Sunscreen Full Coverage Deep Deep Honey Deep Bronze Neutral Deep Deep Mocha Tan Cool Rich Cool Deep Cool Neutral Rich	HOMOSALATE, OCTISALATE AND OCTOCRYLENE	LOreal USA Products Inc	2a44a019-0cc0-439b-aaa5-37582ec5492e	2026-05-14	Warnings	Exact identifier application number: M
THORACOL	HONEY LEMON COUGH DROPS	HART Health	fee9f594-c619-4d77-bb52-632078e0254e	2026-04-16	Warnings	Exact identifier application number: M
First Aid and Burn	BENZALKONIUM CHLORIDE, LIDOCAINE	HART Health	07d447f1-469c-4e34-b807-ede9a449e6ab	2026-04-15	Warnings	Exact identifier application number: M
HYDROCORTISONE	HYDROCORTISONE CREAM	HART Health	c76fb030-cbb5-4773-aa52-d038cb41d0af	2026-04-15	Warnings	Exact identifier application number: M
Hydrogen Peroxide	HYDROGEN PEROXIDE	Amazon.com Services LLC	55b0d905-fcc0-40ba-a5dd-331a27a3a209	2026-04-07	Warnings, Adverse reactions	Exact identifier application number: M
Docusate Sodium	DOCUSATE SODIUM 100MG	Pharbest Pharmaceuticals, Inc.	025e03e0-e273-47ed-87f7-98e388abe047	2026-03-05	Warnings	Exact identifier application number: M
TEENY TUMMY Gas Relief Drops	SIMETHICONE	ALTANTIC BIOLOGICAS CORP.	05eadb73-4468-4dae-a67b-133d893feed2	2026-02-13	Warnings	Exact identifier application number: M
Relief-PE	ACETAMINOPHEN, PHENYLEPHRINE, CHLORPHENIRAMINE	HART Health	9475fb51-931b-4a89-be6b-62e715d0883e	2026-01-15	Warnings	Exact identifier application number: M
ASPIRIN	ASPIRIN	HART Health	a1c73edf-861d-478b-9d3c-0eddcc6879cc	2026-01-14	Warnings	Exact identifier application number: M
HISTAPRIN	DIPHENHYDRAMINE	NorMed	38786a65-a12b-4479-b63c-b7c15410da04	2026-01-14	Warnings	Exact identifier application number: M
Blood Clotting	BENZETHONIUM CHLORIDE AND LIDOCAINE	HART Health	21668731-8b8a-404f-80ab-962a0a9d5f63	2026-01-14	Warnings	Exact identifier application number: M
Bandage	BENZOCAINE AND BENZETHONIUM CHLORIDE	HART Health	6de57472-6dd0-43b6-8a82-fe459fa99ddb	2026-01-14	Warnings	Exact identifier application number: M
Sooth-a-Sting	BENZOCAINE, ISOPROPYL ALCOHOL	HART Health	c0e7d661-a9c9-4656-a516-57552848ebe8	2026-01-12	Warnings	Exact identifier application number: M
Alcohol	ISOPROPYL ALCOHOL	HART Health	8d01b10b-7916-420e-9d44-ebd3806fe315	2026-01-12	Warnings	Exact identifier application number: M
Eye Clean	EYE WASH	HART Health	41f53e2e-c2bc-4bf1-a541-3bcb2cf63002	2025-12-31	Warnings	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