Health Mart Stomach relief

Product NDC: 62011-0140
11-digit product format: 620110140
Labeler code: 62011
Product ID: 62011-0140_d06c11f3-cd7a-4c20-a0a8-013bef76bddf
Type: HUMAN OTC DRUG
Nonproprietary name: Bismuth subsalicylate
Dosage form: TABLET, CHEWABLE
Route: ORAL
Labeler: Strategic Sourcing Services LLC
Application: part335
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2019-10-17
Marketing end: 0000-00-00
Substance: BISMUTH SUBSALICYLATE
Active strength: 262 mg/1
NDC exclude flag: No
Listing certified through: 2023-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	62011-0140		D	Discontinued by firm		2026-10-15
excluded package	package	62011-0140	62011-0140-1	D	Discontinued by firm		2026-10-15

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 · 14 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	62011-0140-1	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	62011-0140-1	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	62011-0140-1	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	62011-0140-1	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	62011-0140-1	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	62011-0140-1	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62011-0140-1	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
62011-0140-1	EA - Each	62011-0140	7ca12609-8dcd-4870-9563-e31880965acc	1	2013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BISMUTH SUBSALICYLATE	ACTIVE INGREDIENT	62TEY51RR1	HEALTH MART STOMACH RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [MCKESSON]	1
BISMUTH SUBSALICYLATE	ACTIVE MOIETY	62TEY51RR1	HEALTH MART STOMACH RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [MCKESSON]	1
CALCIUM CARBONATE	INACTIVE INGREDIENT	H0G9379FGK	HEALTH MART STOMACH RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [MCKESSON]	1
D&C RED NO. 27	INACTIVE INGREDIENT	2LRS185U6K	HEALTH MART STOMACH RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [MCKESSON]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	HEALTH MART STOMACH RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [MCKESSON]	1
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	HEALTH MART STOMACH RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [MCKESSON]	1
SACCHARIN SODIUM DIHYDRATE	INACTIVE INGREDIENT	SB8ZUX40TY	HEALTH MART STOMACH RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [MCKESSON]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	HEALTH MART STOMACH RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [MCKESSON]	1

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
62011-0140-1	62011014001	5 BLISTER PACK in 1 CARTON (62011-0140-1) > 6 TABLET, CHEWABLE in 1 BLISTER PACK	5 blister pack	2019-10-17	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Health Mart Stomach Relief Tablets	Strategic Sourcing Services LLC \| Guardian Drug Company	2025-01-17	HUMAN OTC DRUG LABEL	9