Di

OTC products · Product label record

Digestive Relief Regular Strength drug information

BISMUTH SUBSALICYLATE
TARGET Corporation · ORAL

Product NDC: 11673-372

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameBISMUTH SUBSALICYLATE
Labeler / manufacturerTARGET Corporation
RouteORAL
Drug classBismuth
Product NDC11673-372
Label effective date2026-09-09

Official product label reference

Digestive Relief Regular Strength — TARGET Corporation

This page contains 15 source sections for BISMUTH SUBSALICYLATE, oral route. Label set 90b0c541-2834-4ed7-9d01-76080dd73057, version 9.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

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

Purpose

Purpose Upset stomach reliever/Antidiarrheal
Dosage and administration — label text
Directions shake well before using mL = milliliter measure only with dosing cup provided. do not use any other dosng device. keep dosing cup with product adults and children 12 years and over 30 mL (1 dose) every 1/2 to 1 hour as needed do not exceed 8 doses (240 mL) in 24 hours use until diarrhea stops but not more than 2 days children under 12 years of age: ask a doctor drink plenty of clear fluids to help prevent dehydration caused by diarrhea
Warnings
Warnings Reye's syndrome : Children and teenagers who have or are recovering from chicken pox or flu-like symptoms ahould 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 allergic to salicylates (including aspirin) taking other salicylate products Do not use if you have an ulcer a bleeding problem bloody or black stool Ask a doctor before use if you have fever mucus in the stool Ask a doctor or pharmacist before use if you are taking any drug for diabetes gout arthritis anticoagulation (thinning the blood) When using this product a temporary, but harmless, darkening of the stool and/or tongue may occur. Stop use and ask a doctor if symptoms get worse or last more than 2 days ringing in the ears or loss of hearing occurs diarrhea lasts more than 2 days If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of childen. In case of overdose, get medical help or contact a Posion Control Center right away. (1-800-222-1222)
Active ingredient
Active ingredient (in each 30 mL) Bismuth subsalicylate 525 mg
Do not use
Do not use if you have an ulcer a bleeding problem bloody or black stool
Ask a doctor before use
Ask a doctor before use if you have fever mucus in the stool
Ask a doctor or pharmacist
Ask a doctor or pharmacist before use if you are taking any drug for diabetes gout arthritis anticoagulation (thinning the blood)
While using this medicine
When using this product a temporary, but harmless, darkening of the stool and/or tongue may occur.
When to stop use and seek help
Stop use and ask a doctor if symptoms get worse or last more than 2 days ringing in the ears or loss of hearing occurs diarrhea lasts more than 2 days
Pregnancy or breast feeding
If pregnant or breast-feeding, ask a health professional before use.
Child safety
Keep out of reach of childen. In case of overdose, get medical help or contact a Posion Control Center right away. (1-800-222-1222)
Storage and handling
Other information each 30 mL contains: potassium 8 mg sodium 9 mg each 30 mL contains: salicylate 243 mg low sodium keep tightly closed protect from freezing avoid excessive heat (over 104ºF or 40ºC)
Inactive ingredient
Inactive ingredients benzoic acid, D&C red #22, D&C red #28, flavor, magnesium aluminum silicate, methylcellulose, purified water, saccharin sodium, salicylic acid, sodium salicylate, sorbic acid
Questions
Questions? Call 1-800-910-6874

Official sources and product identifiers

Substances listed: BISMUTH SUBSALICYLATE

RxNorm identifiers: 308762

Package NDC codes

11673-372-16, 11673-372-08

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.