pepto relief

Generic: bismuth subsalicylate

Labeler: advance pharmaceutical inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name pepto relief
Generic Name bismuth subsalicylate
Labeler advance pharmaceutical inc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

bismuth subsalicylate 262 mg/1

Manufacturer
Advance Pharmaceutical Inc.

Identifiers & Regulatory

Product NDC 17714-045
Product ID 17714-045_60f4322f-5cb1-096a-e053-2a91aa0a64eb
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH FINAL
Application Number part335
Listing Expiration 2026-12-31
Marketing Start 2002-01-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 17714045
Hyphenated Format 17714-045

Supplemental Identifiers

RxCUI
308761
UPC
0017714045302
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 pepto relief (source: ndc)
Generic Name bismuth subsalicylate (source: ndc)
Application Number part335 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 262 mg/1
source: ndc
Packaging
  • 30 TABLET, CHEWABLE in 1 BOTTLE (17714-045-30)
source: ndc

Packages (1)

17714-045-30 30 TABLET, CHEWABLE in 1 BOTTLE (17714-045-30)

Ingredients (1)

bismuth subsalicylate (262 mg/1)

Linked Drug Pages (1)

Pepto Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "60f4322f-5cb1-096a-e053-2a91aa0a64eb", "openfda": {"nui": ["M0002611", "N0000180183"], "upc": ["0017714045302"], "unii": ["62TEY51RR1"], "rxcui": ["308761"], "spl_set_id": ["a02babe7-9255-44c7-90e1-b5ad5e59c72a"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, CHEWABLE in 1 BOTTLE (17714-045-30)", "package_ndc": "17714-045-30", "marketing_start_date": "20020109"}], "brand_name": "Pepto Relief", "product_id": "17714-045_60f4322f-5cb1-096a-e053-2a91aa0a64eb", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "17714-045", "generic_name": "Bismuth subsalicylate", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pepto Relief", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "part335", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20020109", "listing_expiration_date": "20261231"}