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Kroger Digestive Relief drug information

BISMUTH SUBSALICYLATE
KROGER COMPANY · ORAL

Product NDC: 30142-524

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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 / manufacturerKROGER COMPANY
RouteORAL
Drug classBismuth
Product NDC30142-524
Label effective date2026-09-01

Official product label reference

Kroger Digestive Relief — KROGER COMPANY

This page contains 17 source sections for BISMUTH SUBSALICYLATE, oral route. Label set 2b32bee7-154a-4e5b-a811-066d1e6c5dcb, 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 anti-diarrheal
Dosage and administration — label text
Directions ▪ swallow with water, do not chew ▪ adults and children 12 years and older: 2 caplets every 1/2 to 1 hour as needed ▪ do not exceed 8 doses (16 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
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 immediately at 1-800-222-1222
Active ingredient
Drug Facts Active ingredient (in each caplet) Bismuth subsalicylate 262 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.
Overdose information
In case of overdose, get medical help or contact a Poison Control Center immediately at 1-800-222-1222
Other safety information
Other Information ▪ each caplet contains: calcium 27 mg, sodium 3 mg ▪ salicylate 99 mg ▪ low sodium ▪ sugar free ▪ store at room temperature.
Questions
Questions or comments? 1-800-632-6900 Inactive Ingredients calcium carbonate, crospovidone, D&C Red No. 27, magnesium stearate, maltodextrin, microcrystalline cellulose, sodium lauryl sulfate.
Inactive ingredient
Inactive Ingredients calcium carbonate, crospovidone, D&C Red No. 27, magnesium stearate, maltodextrin, microcrystalline cellulose, sodium lauryl sulfate.
Package label principal display panel
Table text from source: | IMPORTANT: KEEP THIS CARTON FOR FUTURE REFERENCE ON FULL LABELING

Official sources and product identifiers

Substances listed: BISMUTH SUBSALICYLATE

RxNorm identifiers: 308760

Package NDC codes

30142-524-24

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.