rexall bismuth

Product NDC: 55910-469
Requested package NDC: 55910-469-65
11-digit product format: 559100469
Labeler code: 55910
Product ID: 55910-469_aa37400b-1537-4d3b-9264-1ee62815aafe
Type: HUMAN OTC DRUG
Nonproprietary name: Bismuth subsalicylate
Dosage form: TABLET, CHEWABLE
Route: ORAL
Labeler: Dolgencorp Inc
Application: part335
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2012-09-28
Marketing end: 0000-00-00
Substance: BISMUTH SUBSALICYLATE
Active strength: 262 mg/1
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	55910-469	55910-469-65	D	Discontinued by firm		2026-08-07

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, 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…`
2025-08-27 00:01 UTC · source 2025-08-26	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55910-469-65	2025-06-24	C162847	48780-1	2cef2736-b007-d83d-e063-dadaa90ab31f	Dolgencorp, LLC Bismuth Tabs Drug Facts
55910-469-65	2025-01-30	C162847	48780-1	2cef2736-b007-d83d-e063-dadaa90ab31f	Dolgencorp, LLC Bismuth Tabs Drug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BISMUTH SUBSALICYLATE	ACTIVE INGREDIENT	62TEY51RR1	REXALL BISMUTH (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP INC]	2
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	REXALL BISMUTH (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP INC]	2
CALCIUM CARBONATE	INACTIVE INGREDIENT	H0G9379FGK	REXALL BISMUTH (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP INC]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	REXALL BISMUTH (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP INC]	2
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	REXALL BISMUTH (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP INC]	2
SACCHARIN SODIUM DIHYDRATE	INACTIVE INGREDIENT	SB8ZUX40TY	REXALL BISMUTH (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP INC]	2
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	REXALL BISMUTH (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP INC]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55910-469	REXALL BISMUTH (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP INC]	3	Legacy NDC	20160625_cf38b140-a2d0-4970-8cb8-983b96559f69.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
55910-469-65	55910046965	15 BLISTER PACK in 1 CARTON (55910-469-65) > 2 TABLET, CHEWABLE in 1 BLISTER PACK	15 blister pack	2012-09-28	0000-00-00	No	No	Current