ultra strength digestive relief

Generic: bismuth subsalicylate

Labeler: the kroger co.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ultra strength digestive relief
Generic Name bismuth subsalicylate
Labeler the kroger co.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bismuth subsalicylate 525 mg/1

Manufacturer
THE KROGER CO.

Identifiers & Regulatory

Product NDC 30142-138
Product ID 30142-138_3b873634-dbad-e0bc-e063-6294a90a5f74
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M008
Listing Expiration 2026-12-31
Marketing Start 2019-11-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 30142138
Hyphenated Format 30142-138

Supplemental Identifiers

RxCUI
1998447
UPC
0041260008542
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 strength digestive relief (source: ndc)
Generic Name bismuth subsalicylate (source: ndc)
Application Number M008 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 525 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (30142-138-24) / 24 TABLET in 1 BOTTLE
source: ndc

Packages (1)

30142-138-24 1 BOTTLE in 1 CARTON (30142-138-24) / 24 TABLET in 1 BOTTLE

Ingredients (1)

bismuth subsalicylate (525 mg/1)

Linked Drug Pages (1)

Ultra Strength digestive relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b873634-dbad-e0bc-e063-6294a90a5f74", "openfda": {"nui": ["M0002611", "N0000180183"], "upc": ["0041260008542"], "unii": ["62TEY51RR1"], "rxcui": ["1998447"], "spl_set_id": ["5e288108-1578-4379-a3d6-44b447187643"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["THE KROGER CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-138-24)  / 24 TABLET in 1 BOTTLE", "package_ndc": "30142-138-24", "marketing_start_date": "20191118"}], "brand_name": "Ultra Strength digestive relief", "product_id": "30142-138_3b873634-dbad-e0bc-e063-6294a90a5f74", "dosage_form": "TABLET", "product_ndc": "30142-138", "generic_name": "Bismuth subsalicylate", "labeler_name": "THE KROGER CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Strength digestive relief", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "525 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191118", "listing_expiration_date": "20261231"}