Home NDC 17714-045 Pepto Relief
Product NDC 17714-045
11-digit product format 177140045
Labeler code 17714
Product ID 17714-045_60f4322f-5cb1-096a-e053-2a91aa0a64eb
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Advance Pharmaceutical Inc.
Application part335
Marketing category OTC MONOGRAPH FINAL
Marketing start 2002-01-09
Substance BISMUTH SUBSALICYLATE
Active strength 262 mg/1
Pharmacologic classes Bismuth [CS], Bismuth [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Pepto Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBSALICYLATE 262 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 62TEY51RR1 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308761 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 17714-045-30 Pepto Relief 30 in 1 BOTTLE TABLET, CHEWABLE 30 2
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BISMUTH SUBSALICYLATE ACTIVE INGREDIENT 62TEY51RR1 PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1 BISMUTH CATION ACTIVE MOIETY ZS9CD1I8YE PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1 CALCIUM CARBONATE INACTIVE INGREDIENT H0G9379FGK PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1 CHERRY INACTIVE INGREDIENT BUC5I9595W PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1 D&C RED NO. 27 INACTIVE INGREDIENT 2LRS185U6K PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1 DEXTROSE INACTIVE INGREDIENT IY9XDZ35W2 PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17714-045 PEPTO RELIEF (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [ADVANCE PHARMACEUTICAL INC.] 2 Current NDC, Legacy NDC, 1 package rows 20171223_a02babe7-9255-44c7-90e1-b5ad5e59c72a.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 17714-045-30 17714004530 30 TABLET, CHEWABLE in 1 BOTTLE (17714-045-30) 2002-01-09 0000-00-00 No No Current