up and up 5-symptom digestive relief
Generic: bismuth subsalicylate
Labeler: target corporationDrug Facts
Product Profile
Brand Name
up and up 5-symptom digestive relief
Generic Name
bismuth subsalicylate
Labeler
target corporation
Dosage Form
TABLET
Routes
Active Ingredients
bismuth subsalicylate 262 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
11673-122
Product ID
11673-122_42c2f050-6c70-6c79-e063-6394a90ade8f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M008
Listing Expiration
2026-12-31
Marketing Start
2019-03-12
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673122
Hyphenated Format
11673-122
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
up and up 5-symptom 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
- 48 TABLET in 1 BOTTLE, PLASTIC (11673-122-48)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42c2f050-6c70-6c79-e063-6394a90ade8f", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["308760"], "spl_set_id": ["7f6b2960-943d-464c-9ff9-4649a8ab4a4e"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "48 TABLET in 1 BOTTLE, PLASTIC (11673-122-48)", "package_ndc": "11673-122-48", "marketing_start_date": "20190312"}], "brand_name": "up and up 5-symptom digestive relief", "product_id": "11673-122_42c2f050-6c70-6c79-e063-6394a90ade8f", "dosage_form": "TABLET", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "11673-122", "generic_name": "Bismuth subsalicylate", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up 5-symptom digestive relief", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}