Stomach Relief

Product NDC: 55319-842
Requested package NDC: 55319-842-08
11-digit product format: 553190842
Labeler code: 55319
Product ID: 55319-842_d0a9c99c-905a-49e3-a3c2-857efedc9d2d
Type: HUMAN OTC DRUG
Nonproprietary name: Bismuth subsalicylate
Dosage form: LIQUID
Route: ORAL
Labeler: Family Dollar (FAMILY WELLNESS)
Application: part335
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2019-02-28
Marketing end: 0000-00-00
Substance: BISMUTH SUBSALICYLATE
Active strength: 525 mg/15mL
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	55319-842	55319-842-08	D	Discontinued by firm		2026-10-05

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 · 4 matching rows.

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

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2022-08-30 03:57 UTC · source 2022-08-29	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

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
55319-842-08	2023-01-25	C162847	48780-1	d6a99b39-9e6d-a426-e053-dadaa90af4c2	Drug Facts
55319-842-08	2022-01-28	C162847	48780-1	d6a99b39-9e6d-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55319-842	STOMACH RELIEF ULTRA (BISMUTH SUBSALICYLATE) LIQUID [FAMILY DOLLAR (FAMILY WELLNESS)]	2	Legacy NDC	20230126_0ab030be-e563-44df-9a7e-9e5fd6b87416.zip

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55319-842-08	55319084208	237 mL in 1 BOTTLE, PLASTIC (55319-842-08)	237 ml	2019-02-28	0000-00-00	No	No	Current