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 / manufacturerWalmart Inc.
RouteORAL
Drug classBismuth
Product NDC79903-443
Label effective date2026-08-29
Official product label reference
Regular Strength Stomach Relief — Walmart Inc.
This page contains 16 source sections for BISMUTH SUBSALICYLATE, oral route. Label set 50a88db4-633d-d3bc-e063-6294a90a18c5, version 2.
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 -belching -fullness
Purpose
Purpose Upset stomach reliever and antidiarrheal
Dosage and administration — label text
Directions shake well before use only use dose cup provided adults and children 12 years and over: - 30 mL (1 dose) every ½ hour or 60 mL (2 doses) every hour as needed for diarrhea / travelers’ diarrhea - 30 mL (1 dose) every ½ hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea) do not exceed 8 doses (240 mL) 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
Warnings
Warnings Reye’s syndrome: 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 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 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 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 children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Unclassified section
Drug Facts
Active ingredient
Active ingredient (in each 30 mL dose) 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 anticoagulation (thinning the blood) diabetes gout arthritis
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 children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Storage and handling
Other information each 30 mL dose contains: salicylate 199 mg keep tightly closed protect from freezing avoid excessive heat (over 104°F or 40°C)
Inactive ingredient
Inactive ingredients benzoic acid, D&C red no. 22, D&C red no. 28, flavor, glycerin, purified water, sucralose, xanthan gum
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.