stomach relief

Generic: bismuth subsalicylate

Labeler: cardinal health 110, llc. dba leader
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name stomach relief
Generic Name bismuth subsalicylate
Labeler cardinal health 110, llc. dba leader
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

bismuth subsalicylate 262 mg/1

Manufacturer
CARDINAL HEALTH 110, LLC. DBA LEADER

Identifiers & Regulatory

Product NDC 70000-0591
Product ID 70000-0591_227d63ba-9ab8-4895-9ba1-7b3c9e2100d3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M008
Listing Expiration 2026-12-31
Marketing Start 2021-10-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 700000591
Hyphenated Format 70000-0591

Supplemental Identifiers

RxCUI
308761
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 stomach relief (source: ndc)
Generic Name bismuth subsalicylate (source: ndc)
Application Number M008 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 262 mg/1
source: ndc
Packaging
  • 5 BLISTER PACK in 1 BOX (70000-0591-1) / 6 TABLET, CHEWABLE in 1 BLISTER PACK
  • 8 BLISTER PACK in 1 BOX (70000-0591-2) / 6 TABLET, CHEWABLE in 1 BLISTER PACK
source: ndc

Packages (2)

70000-0591-1 5 BLISTER PACK in 1 BOX (70000-0591-1) / 6 TABLET, CHEWABLE in 1 BLISTER PACK 70000-0591-2 8 BLISTER PACK in 1 BOX (70000-0591-2) / 6 TABLET, CHEWABLE in 1 BLISTER PACK

Ingredients (1)

bismuth subsalicylate (262 mg/1)

Linked Drug Pages (1)

Stomach Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "227d63ba-9ab8-4895-9ba1-7b3c9e2100d3", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["308761"], "spl_set_id": ["b38d815b-a249-46d1-a9d0-4e8efab3e56b"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC. DBA LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 BLISTER PACK in 1 BOX (70000-0591-1)  / 6 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "70000-0591-1", "marketing_start_date": "20211005"}, {"sample": false, "description": "8 BLISTER PACK in 1 BOX (70000-0591-2)  / 6 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "70000-0591-2", "marketing_start_date": "20211005"}], "brand_name": "Stomach Relief", "product_id": "70000-0591_227d63ba-9ab8-4895-9ba1-7b3c9e2100d3", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "70000-0591", "generic_name": "Bismuth subsalicylate", "labeler_name": "CARDINAL HEALTH 110, LLC. DBA LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stomach Relief", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211005", "listing_expiration_date": "20261231"}