pepto bismol diarrhea liquicaps

Generic: bismuth subsalicylate

Labeler: the procter & gamble manufacturing company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pepto bismol diarrhea liquicaps
Generic Name bismuth subsalicylate
Labeler the procter & gamble manufacturing company
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

bismuth subsalicylate 262 mg/1

Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 37000-537
Product ID 37000-537_0b3cb53e-1d79-f343-e063-6394a90a17ca
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M008
Marketing Start 2018-03-01
Marketing End 2026-06-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37000537
Hyphenated Format 37000-537

Supplemental Identifiers

RxCUI
2121072 2121074
UPC
0301490001714
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 bismol diarrhea liquicaps (source: ndc)
Generic Name bismuth subsalicylate (source: ndc)
Application Number M008 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 262 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (37000-537-12) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (37000-537-48) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (2)

37000-537-12 1 BLISTER PACK in 1 CARTON (37000-537-12) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 37000-537-48 4 BLISTER PACK in 1 CARTON (37000-537-48) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (1)

bismuth subsalicylate (262 mg/1)

Linked Drug Pages (1)

Pepto Bismol Diarrhea Liquicaps ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0b3cb53e-1d79-f343-e063-6394a90a17ca", "openfda": {"nui": ["M0002611", "N0000180183"], "upc": ["0301490001714"], "unii": ["62TEY51RR1"], "rxcui": ["2121072", "2121074"], "spl_set_id": ["851997d7-cb82-17bf-e053-2a91aa0ab78b"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (37000-537-12)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "37000-537-12", "marketing_end_date": "20260630", "marketing_start_date": "20190301"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (37000-537-48)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "37000-537-48", "marketing_end_date": "20260630", "marketing_start_date": "20190301"}], "brand_name": "Pepto Bismol Diarrhea Liquicaps", "product_id": "37000-537_0b3cb53e-1d79-f343-e063-6394a90a17ca", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "37000-537", "generic_name": "Bismuth subsalicylate", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pepto Bismol", "brand_name_suffix": "Diarrhea Liquicaps", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260630", "marketing_start_date": "20180301"}