NDC 55910-637 – Ultra Bismuth

Bismuth Subsalicylate 525 mg/15mL · Liquid · Oral

Human Otc Drug

Product NDC55910-637

Product details

Brand name
Ultra Bismuth
Generic name
Bismuth subsalicylate
Labeler
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Dosage form
Liquid
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M008
Marketed since
November 29, 2019
Listing expires
December 31, 2026
Pharmacologic class
Bismuth

Active ingredients

Uses, dosage, side effects and warnings for Ultra Bismuth →

Package NDC codes (2)

Package NDCDescriptionSince
55910-637-04118 mL in 1 BOTTLE, PLASTIC (55910-637-04)Nov 29, 2019
55910-637-12355 mL in 1 BOTTLE, PLASTIC (55910-637-12)Nov 29, 2019