ultra bismuth

Generic: bismuth subsalicylate

Labeler: dolgencorp, inc. (dollar general & rexall)
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ultra bismuth
Generic Name bismuth subsalicylate
Labeler dolgencorp, inc. (dollar general & rexall)
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

bismuth subsalicylate 525 mg/15mL

Manufacturer
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)

Identifiers & Regulatory

Product NDC 55910-637
Product ID 55910-637_c751324d-47d9-49f0-b941-a526747e71c3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M008
Listing Expiration 2026-12-31
Marketing Start 2019-11-29

Pharmacologic Class

Established (EPC)
bismuth [epc]
Chemical Structure
bismuth [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55910637
Hyphenated Format 55910-637

Supplemental Identifiers

RxCUI
308763
UNII
62TEY51RR1
NUI
M0002611 N0000180183

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ultra bismuth (source: ndc)
Generic Name bismuth subsalicylate (source: ndc)
Application Number M008 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 525 mg/15mL
source: ndc
Packaging
  • 118 mL in 1 BOTTLE, PLASTIC (55910-637-04)
  • 355 mL in 1 BOTTLE, PLASTIC (55910-637-12)
source: ndc

Packages (2)

55910-637-04 118 mL in 1 BOTTLE, PLASTIC (55910-637-04) 55910-637-12 355 mL in 1 BOTTLE, PLASTIC (55910-637-12)

Ingredients (1)

bismuth subsalicylate (525 mg/15mL)

Linked Drug Pages (1)

Ultra Bismuth ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c751324d-47d9-49f0-b941-a526747e71c3", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["308763"], "spl_set_id": ["0fc01a1a-4b1d-4c78-9955-220984a8019c"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, PLASTIC (55910-637-04)", "package_ndc": "55910-637-04", "marketing_start_date": "20191129"}, {"sample": false, "description": "355 mL in 1 BOTTLE, PLASTIC (55910-637-12)", "package_ndc": "55910-637-12", "marketing_start_date": "20191129"}], "brand_name": "Ultra Bismuth", "product_id": "55910-637_c751324d-47d9-49f0-b941-a526747e71c3", "dosage_form": "LIQUID", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "55910-637", "generic_name": "Bismuth subsalicylate", "labeler_name": "Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Bismuth", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "525 mg/15mL"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191129", "listing_expiration_date": "20261231"}