Pepto Bismol

Manufacturer
Lil' Drug Store Products, Inc.
Effective date
2023-07-19
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:55:41

Label at a glance#

ProductPepto Bismol
Active ingredientBISMUTH SUBSALICYLATE
Label structure11 sections

Indications and uses

relieves • travelers' diarrhea • diarrhea • upset stomach due to overindulgence in food and drink, including: • heartburn • indigestion • nausea • gas • belching • fullness

Dosage and administration

chew or dissolve in mouth adults and children 12 years and over: 2 tablets (1 dose) every 1/2 hour or 4 tablets (2 doses) every hour as needed for diarrhea 2 tablets (1 dose) every ½ hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea) do not exceed 8 doses (16 tablets) in 24 hours use until diarrhea stops but not more than 2 days children under 12 years: ask a doctor drink plenty of c...

Storage and handling

each tablet contains: calcium 140 mg, magnesium 9 mg salicylate 99 mg low sodium avoid excessive heat (over 104°F or 40°C)

Label contents#

Full prescribing information#

Active Ingredient(in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Bismuth subsalicylate 262 mg

Purpose

OTC - PURPOSE SECTION

Upset stomach reliever and antidiarrheal

Uses

INDICATIONS & USAGE SECTION

relieves

• travelers' diarrhea

• diarrhea

• upset stomach due to overindulgence in food and drink, including:

• heartburn

• indigestion

• nausea

• gas

• belching

• fullness

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

Do not use if you have

OTC - DO NOT USE SECTION

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • fever
  • mucus in the stool

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

OTC - ASK DOCTOR/PHARMACIST SECTION

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

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • symptoms get worse
  • ringing in the ears 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • chew or dissolve in mouth
  • adults and children 12 years and over: 2 tablets (1 dose) every 1/2 hour or 4 tablets (2 doses) every hour as needed for diarrhea
  • 2 tablets (1 dose) every ½ hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea)
  • do not exceed 8 doses (16 tablets) 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 tablet contains: calcium 140 mg, magnesium 9 mg
  • salicylate 99 mg
  • low sodium
  • avoid excessive heat (over 104°F or 40°C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

adipic acid, calcium carbonate, D&C Red No. 27 aluminum lake, FD&C Red No. 40 aluminum lake, flavor, magnesium stearate, mannitol, povidone, saccharin sodium, talc

Questions?

OTC - QUESTIONS SECTION

1-800-717-3786

SPL UNCLASSIFIED SECTION

PRODUCT REPACKAGED AND DISTRIBUTED WITH PERMISSION OF MANUFACTURER BY:

Convenience Valet® Glendale Heights, IL 60139 1-800-351-2000 (8:30 AM - 5:00 PM CST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pepto Bismol
Bismuth Subsalicylate
Upset Stomach Reliever/Antidiarrheal

CHEWABLES

5 SYMPTOM RELIEF

NAUSEA

HEARTBURN

INDIGESTION

UPSET STOMACH

DIARRHEA

4 CHEWABLE TABLETS


PEPTO 4CTPEPTO 4CT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pepto Bismol
Bismuth Subsalicylate
Upset Stomach Reliever/Antidiarrheal

CHEWABLES

5 SYMPTOM RELIEF

NAUSEA

HEARTBURN

INDIGESTION

UPSET STOMACH

DIARRHEA

6 CHEWABLE TABLETS

Pepto 6ctPepto 6ct

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
29485-1531PEPTO BISMOL (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [LIL' DRUG STORE PRODUCTS, INC.]6Legacy NDC20230720_d04e42bf-2748-f12b-e053-2a95a90a35e5.zip
29485-6754PEPTO BISMOL (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [LIL' DRUG STORE PRODUCTS, INC.]6Legacy NDC20230720_d04e42bf-2748-f12b-e053-2a95a90a35e5.zip

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
29485-153129485-1531-4
29485-675429485-6754-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

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
00d86cb8-f8f0-e7e2-e063-6294a90add1dd04e42bf-2748-f12b-e053-2a95a90a35e52023-07-19WarningsExact identifier
spl id: 00d86cb8-f8f0-e7e2-e063-6294a90add1d
spl set id: d04e42bf-2748-f12b-e053-2a95a90a35e5

Reported adverse events (FAERS/openFDA)#

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