ultra strength digestive relief
Generic: bismuth subsalicylate
Labeler: walgreens co.Drug Facts
Product Profile
Brand Name
ultra strength digestive relief
Generic Name
bismuth subsalicylate
Labeler
walgreens co.
Dosage Form
TABLET
Routes
Active Ingredients
bismuth subsalicylate 525 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0363-1302
Product ID
0363-1302_447d20f5-798d-ca2a-e063-6294a90ada0d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M008
Listing Expiration
2026-12-31
Marketing Start
2022-09-26
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03631302
Hyphenated Format
0363-1302
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
ultra strength digestive relief (source: ndc)
Generic Name
bismuth subsalicylate (source: ndc)
Application Number
M008 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 525 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (0363-1302-02) / 24 TABLET 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": "447d20f5-798d-ca2a-e063-6294a90ada0d", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["1998447"], "spl_set_id": ["756e7a47-7e14-4694-84fa-ca6396f7edcc"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["WALGREENS CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1302-02) / 24 TABLET in 1 BOTTLE", "package_ndc": "0363-1302-02", "marketing_start_date": "20220926"}], "brand_name": "Ultra Strength digestive relief", "product_id": "0363-1302_447d20f5-798d-ca2a-e063-6294a90ada0d", "dosage_form": "TABLET", "product_ndc": "0363-1302", "generic_name": "Bismuth subsalicylate", "labeler_name": "WALGREENS 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": "20220926", "listing_expiration_date": "20261231"}