digestive relief
Generic: bismuth subsalicylate
Labeler: safewayDrug Facts
Product Profile
Brand Name
digestive relief
Generic Name
bismuth subsalicylate
Labeler
safeway
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
bismuth subsalicylate 262 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
21130-125
Product ID
21130-125_424aa911-6748-010b-e063-6394a90a7ae7
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M008
Listing Expiration
2026-12-31
Marketing Start
2020-10-05
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
21130125
Hyphenated Format
21130-125
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
digestive relief (source: ndc)
Generic Name
bismuth subsalicylate (source: ndc)
Application Number
M008 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 262 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (21130-125-40) / 40 TABLET, FILM COATED in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "424aa911-6748-010b-e063-6394a90a7ae7", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["308760"], "spl_set_id": ["5538d56a-b258-4260-b51b-f5131bd76885"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["SAFEWAY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-125-40) / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "21130-125-40", "marketing_start_date": "20201005"}], "brand_name": "Digestive Relief", "product_id": "21130-125_424aa911-6748-010b-e063-6394a90a7ae7", "dosage_form": "TABLET, FILM COATED", "product_ndc": "21130-125", "generic_name": "Bismuth Subsalicylate", "labeler_name": "SAFEWAY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Digestive Relief", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201005", "listing_expiration_date": "20261231"}