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Ultra Strength digestive relief drug information

BISMUTH SUBSALICYLATE
THE KROGER CO. · ORAL

Product NDC: 30142-138

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Generic nameBISMUTH SUBSALICYLATE
Labeler / manufacturerTHE KROGER CO.
RouteORAL
Drug classBismuth
Product NDC30142-138
Label effective date2026-09-01

Official product label reference

Ultra Strength digestive relief — THE KROGER CO.

This page contains 16 source sections for BISMUTH SUBSALICYLATE, oral route. Label set 5e288108-1578-4379-a3d6-44b447187643, version 8.

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 ▪ belching ▪ fullness

Purpose

Purpose Upset stomach reliever and antidiarrheal
Dosage and administration — label text
Directions ▪ swallow with water, do not chew ▪ adults and children 12 years and over: 1 caplet (1 dose) every ½ hour or 2 caplets (2 doses) every hour as needed for diarrhea ▪ 1 caplet (1 dose) every ½ hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea) ▪ do not exceed 8 doses (8 caplets) 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 right away.
Unclassified section
Drug Facts
Active ingredient
Active ingredient (in each caplet) 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 right away.
Storage and handling
Other information ▪ each caplet contains: calcium 54 mg ▪ salicylate 199 mg ▪ store at room temperature
Inactive ingredient
Inactive ingredients calcium carbonate, crospovidone, FD&C Red No. 27 Lake, magnesium stearate, microcrystalline cellulose, polysorbate 80.
Questions
Questions? 1-866-467-2748

Official sources and product identifiers

Substances listed: BISMUTH SUBSALICYLATE

RxNorm identifiers: 1998447

Package NDC codes

30142-138-24

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.