up and up 5-symptom digestive relief

Manufacturer
Target Corporation
Effective date
2025-11-04
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:41:58

Label at a glance#

Productup and up 5-symptom digestive relief
Active ingredientBISMUTH SUBSALICYLATE
Label structure8 sections

Dosage and administration

swallow with water, do not chew adults and children 12 years and older: 2 caplets every 1/2 to 1 hour as needed do not exceed 8 doses (16 caplets) in 24 hours use until diarrhea stops but not more than 2 days children under 12 years: ask a doctor drink plenty of clear fluids to help prevent dehydration caused by diarrhea

Storage and handling

each caplet contains: calcium 27 mg sodium 3 mg salicylate 99 mg low sodium sugar free avoid excessive heat (over 104°F or 40°C)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each caplet)

OTC - ACTIVE INGREDIENT SECTION

Bismuth subsalicylate 262 mg

Purpose

OTC - PURPOSE SECTION

Upset stomach reliever and anti-diarrheal

Uses

INDICATIONS & USAGE SECTION

relieves

  • heartburn
  • indigestion
  • nausea
  • upset stomach
  • diarrhea

Warnings

WARNINGS SECTION

Reye's syndrome

SPL UNCLASSIFIED SECTION

Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

Allergy alert:

SPL UNCLASSIFIED SECTION

Contains salicylate. Do not take if you are

  • allergic to salicylates (including aspirin)
  • taking other salicylate products

OTC - DO NOT USE SECTION

Do not use ifyou have

  • an ulcer
  • a bleeding problem
  • bloody or black stool

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • fever
  • mucus in the stool

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor before use if you are taking any drug for

  • anticoagulation (thinning of the blood)
  • diabetes
  • gout
  • arthritis

OTC - WHEN USING SECTION

When using this producta temporary, but harmless, darkening of the stool and/or tongue may occur.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • symptoms get worse or last more than 2 days
  • ringing in the ears occurs or loss of hearing occurs
  • diarrhea lasts more than 2 days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding,ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately.1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

  • swallow with water, do not chew
  • adults and children 12 years and older:2 caplets every 1/2 to 1 hour as needed
  • do not exceed 8 doses (16 caplets) in 24 hours
  • use until diarrhea stops but not more than 2 days
  • children under 12 years:ask a doctor
  • drink plenty of clear fluids to help prevent dehydration caused by diarrhea

Other information

STORAGE AND HANDLING SECTION

  • each caplet contains:calcium 27 mg
  • sodium 3 mg
  • salicylate 99 mg
  • low sodium
  • sugar free
  • avoid excessive heat (over 104°F or 40°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

calcium carbonate, crospovidone, D&C red#27 aluminum lake, magnesium stearate, microcrystalline cellulose, sodium lauryl sulfate.

PRINCIPAL DISPLAY PANEL -

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 11673-125-20

Compare toactive ingredient in Pepto-Bismol® Caplets*

5- symptom digestive relief

relief of upset stomach, nausea, heartburn, indigestion, diarrhea

40 CAPLETS

*This product is not manufactured or distributed by Procter & Gamble Inc. the distributor of PEPTO-BISMOL®

TAMPER EVIDENT DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING.

245 05 0375 R01 ID285492

Dist.by Target Corp., Mpls ., MN 55403

©2017 Target Brands, Inc.

Shop Target.com

Guest Services 1-800-910-6874

up and up 5-symptom digestive relief bismuth subsalicylate,262 mg/antidiarrheal Caplet
up and up 5-symptom digestive relief bismuth subsalicylate,262 mg/antidiarrheal Caplet

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308760bismuth subsalicylate 262 MG Oral TabletPSN9
308760bismuth subsalicylate 262 MG Oral TabletSCD9

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15Product name120240313
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-125-20up and up 5-symptom digestive relief40 in 1 BOTTLE, PLASTICTABLET409

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
11673-125-20EA - Each11673-1254941bd3d-3943-45f9-ab31-983bfdd5d11012016-05-16

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-12511673-125-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82024-11-07full-release2026-06-01 00:35:38

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
up and up 5-symptom digestive reliefBISMUTH SUBSALICYLATETarget Corporation6462e224-5ee7-4556-90f2-994eaf89b71b2025-11-04WarningsExact identifier
ndc (package): 11673-125-20
ndc (product): 11673-125
ndc11 (package): 11673012520
spl id: 42c36460-f332-0c52-e063-6394a90af168
spl set id: 6462e224-5ee7-4556-90f2-994eaf89b71b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.