stomach relief ultra strength

Generic: bismuth subsalicylate

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name stomach relief ultra strength
Generic Name bismuth subsalicylate
Labeler p & l development, llc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

bismuth subsalicylate 525 mg/15mL

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 49580-0842
Product ID 49580-0842_2098abda-1027-4fc4-b273-2a0f39316a41
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M008
Listing Expiration 2026-12-31
Marketing Start 2019-02-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 495800842
Hyphenated Format 49580-0842

Supplemental Identifiers

RxCUI
308763
UPC
0349580842090
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 ultra strength (source: ndc)
Generic Name bismuth subsalicylate (source: ndc)
Application Number M008 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 525 mg/15mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE, PLASTIC (49580-0842-8)
source: ndc

Packages (1)

49580-0842-8 237 mL in 1 BOTTLE, PLASTIC (49580-0842-8)

Ingredients (1)

bismuth subsalicylate (525 mg/15mL)

Linked Drug Pages (1)

Stomach Relief Ultra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2098abda-1027-4fc4-b273-2a0f39316a41", "openfda": {"nui": ["M0002611", "N0000180183"], "upc": ["0349580842090"], "unii": ["62TEY51RR1"], "rxcui": ["308763"], "spl_set_id": ["cb5ca7ab-39cf-4b07-ac22-a00b214db102"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (49580-0842-8)", "package_ndc": "49580-0842-8", "marketing_start_date": "20190228"}], "brand_name": "Stomach Relief Ultra Strength", "product_id": "49580-0842_2098abda-1027-4fc4-b273-2a0f39316a41", "dosage_form": "LIQUID", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "49580-0842", "generic_name": "Bismuth subsalicylate", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stomach Relief", "brand_name_suffix": "Ultra Strength", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "525 mg/15mL"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190228", "listing_expiration_date": "20261231"}