CVS Health Anti-Diarrheal

Manufacturer
CVS Pharmacy,Inc.
Effective date
2026-08-17
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
daily-update
Hydrated at
2026-08-19 00:02:16

Label at a glance#

ProductCVS Health Anti-Diarrheal Vanilla
Active ingredientBismuth subsalicylate
Label structure9 sections

Indications and uses

relieves ▪ traveler’s diarrhea ▪ diarrhea ▪ upset stomach due to overindulgence in food and drink ▪ heartburn ▪ indigestion ▪ nausea ▪ gas

Dosage and administration

• shake well immediately before each use • adults and children 12 years of age and older: 30 ml or 2 tablespoonful • for accurate dosing, use convenient pre-measured dose cup • repeat dose every 1/2 hour to 1 hour as needed • do not exceed 8 doses 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...

Storage and handling

• each 15mL tablespoon contains: sodium 10 mg • each 15mL tablespoon contains: salicylate 130 mg • do not use if printed inner seal is broken or missing • store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient (in each 15 ml)

OTC - ACTIVE INGREDIENT SECTION

Bismuth Subsalicylate 262 mg

Purposes

OTC - PURPOSE SECTION

Antidiarrheal/Upset stomach reliever

Uses

INDICATIONS & USAGE SECTION

relieves

  • traveler’s diarrhea
  • diarrhea
  • upset stomach due to overindulgence in food and drink
  • heartburn
  • indigestion
  • nausea
  • gas

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: Contains salicylate. Do not take if you are

SPL UNCLASSIFIED SECTION

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

OTC - DO NOT USE SECTION

Do not use if you have

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

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • a sodium-restricted diet
  • fever
  • mucus in the stool

OTC - ASK DOCTOR/PHARMACIST SECTION

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

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

OTC - WHEN USING SECTION

When using this product a 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
  • 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 at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well immediately before each use
  • adults and children 12 years of age and older: 30 ml or 2 tablespoonful
  • for accurate dosing, use convenient pre-measured dose cup
  • repeat dose every 1/2 hour to 1 hour as needed
  • do not exceed 8 doses 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 15mL tablespoon contains: sodium 10 mg
    • each 15mL tablespoon contains: salicylate 130 mg
    • do not use if printed inner seal is broken or missing
    • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

caramel, carboxymethylcellulose sodium, microcrystalline cellulose, natural and artificial flavor, potassium sorbate, salicylic acid , simethicone emulsion, sucralose, sucrose, water, xanthan gum

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

PRINCIPAL DISPLAY PANEL - 355 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50% MORE FREE THAN THE 8 OZ NATIONAL BRAND

CVS Health ™

NDC 59779-883-12

Compare to the active ingredient in Kaopectate®*

Vanilla

Anti-Diarrheal

Bismuth Subsalicylate, 262 mg

Upset stomach reliever

  • Effective diarrhea relief
  • Restores natural balance
  • Contains Salicylates
  • Vanilla

12 FL OZ (355 mL)

Distributed by: CVS Pharmacy, Inc.

One CVS Drive, Woonsocket, RI 02895

© 2017CVS/pharmacy

CVS.com® 1-800-SHOP CVS

V-16415

*This product is not manufactured or distributed by Chattem Inc., the distributor of Kaopectate ®.

CVS Health Anti-Diarrheal
CVS Health Anti-Diarrheal

DailyMed Product Concepts#

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

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59779-88359779-883-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
92025-12-09full-release2026-06-01 01:21:27

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
CVS Health Anti-Diarrheal VanillaBISMUTH SUBSALICYLATECVS Pharmacy,Inc.ce1ed357-228b-452c-9bd4-6b0d20f41c1d2026-08-17WarningsExact identifier
ndc (package): 59779-883-12
ndc (product): 59779-883
ndc11 (package): 59779088312
spl id: 09ba06ca-e638-4428-96fc-291ad02d3425
spl set id: ce1ed357-228b-452c-9bd4-6b0d20f41c1d

Reported adverse events (FAERS/openFDA)#

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