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 / manufacturerUnifirst First Aid Corporation
RouteORAL
Drug classBismuth
Product NDC47682-670
Label effective date2026-09-10
Official product label reference
Medique Diotame Instydose — Unifirst First Aid Corporation
This page contains 15 source sections for BISMUTH SUBSALICYLATE, oral route. Label set 5b214128-6980-0f84-e063-6294a90ad8ca, 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 Uses releives travelers' diarrhea diarrhea upset stomach due to overindulgence in food and drin, including: heartburn indigestion nausea gas belching fullness
Directions Directions shake well before use, only with dosing cup provided drink plenty of clear fluids to help prevent dehydration Adults and children: (12 years and over) 30 mL (1 dose) every 1/2 hour or 60 mL (2 doses) every hour as needed for diarrhea / travelers' diarrhea 30 mL (1 dose) every 1/2 hour as needed for over indulgence (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
Warnings
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 Syndrom, a rare but serious illness. Allergy alert: Contains salicylate. Do not take if you are: allergic to salicylates (including aspirin) taking other salicylate products
When using this product When using this product, a temporary but harmless darkening of the stool and/or tongue may occur
Unclassified section
Drug Facts Drug Facts
Active ingredient
Active Ingredient Active Ingredient Bismuth Subsalicylate 525 mg
Do not use
Do not use if you have 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 Ask a doctor before use if you have fever mucus in the stool
Ask a doctor or pharmacist
Ask a doctor or pharmacist Ask a doctor or pharmacist if you are taking any drug for anticoagulation (thinning of the blood) diabetes gout arthritis
When to stop use and seek help
Stop use and ask a doctor if Stop use and ask a doctor if symptoms get worse or last for 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 If pregnant or breast-feeding, ask a health professional before use.
Child safety
Keep out of reach of children Keep out of reach of children. In case of accidental overdose, contact a physician or poison control center right away (1-800-222-1222).
Other safety information
Other information Other information each 30 mL dose contains: sodium 22 mg, salicylate 249 mg protect from freezing avoid excessive heat (over 104°F or 40°C) TAMPER -EVIDENT FEATURE: Do not use if printed safety seal is torn, broken, or missing.
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.