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Treda ultra - Medication Information

Product NDC Code 83393-749
Drug Name

Treda ultra

Type Brand
Active Ingredients
Bismuth subsalicylate 525 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 1998447
Application Number M008
Labeler Name Laboratorios Sanfer, S.A. de C.V.
Packages
Package NDC Code Description
83393-749-08 1 bottle, plastic in 1 carton (83393-749-08) / 24 tablet in 1 bottle, plastic
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each caplet) Bismuth subsalicylate 525 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions do not take more than directed drink plenty of clear fluids to help prevent dehydration caused by diarrhea swallow with water; do not chew adults and children 12 years and over: 1 caplet every 1/2 to 1 hour as needed. Do not exceed 8 caplets in 24 hours. do not use for more than 2 days unless directed by a doctor use until diarrhea stops, but not more than 2 days children under 12 years: ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients calcium carbonate, corn starch, D&C red #27 aluminum lake, D&C red #30 aluminum lake, magnesium stearate, mannitol, microcrystalline cellulose, povidone, silicon dioxide, sodium starch glycolate, stearic acid

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses relieves travelers’ diarrhea diarrhea upset stomach due to overindulgence in food and drink, including: indigestion fullness gas nausea heartburn belching

Purpose

Information about the drug product’s indications for use.
Purpose Upset stomach reliever/antidiarrheal

Spl product data elements

Usually a list of ingredients in a drug product.
Treda Ultra Bismuth subsalicylate BISMUTH SUBSALICYLATE SALICYLIC ACID BISMUTH CATION CALCIUM CARBONATE STARCH, CORN D&C RED NO. 27 ALUMINUM LAKE D&C RED NO. 30 MAGNESIUM STEARATE MANNITOL MICROCRYSTALLINE CELLULOSE POVIDONE, UNSPECIFIED SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STEARIC ACID 44;749

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Principal display panel Treda® Ultra Bismuth Subsalicylate 525 mg UPSET STOMACH RELIEVER ANTIDIARRHEAL RELIEVES: Diarrhea Nausea Heartburn Upset Stomach Indigestion Actual Size 24 caplets sanfer® TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING 50844 ORG032174908 Manufactured for: Laboratorios Sanfer S.A. de C.V. Blvd. Adolfo López Mateos No. 314 Col. Tlacopac, CDMX, 01049. México This product is produced in compliance with all United States regulatory and quality requirements for pharmaceutical product. Treda Ultra 44-749 Treda Ultra 44-749

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if you have fever mucus in the stool

Ask doctor or pharmacist

Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.
Ask a doctor or pharmacist before use if you are taking any drug for gout diabetes arthritis anticoagulation (thinning the blood)

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use if you have an ulcer a bleeding problem bloody or black stool

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? Call 1-(833) 604-1084 (English and Spanish) 8:00 AM-5:00 PM CST, Monday-Friday

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if symptoms get worse ringing in the ears or loss of hearing occurs diarrhea lasts more than 2 days

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product a temporary, but harmless, darkening of the stool and/or tongue may occur

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health professional before use.

Storage and handling

Information about safe storage and handling of the drug product.
Other information each caplet contains: calcium 45 mg, salicylate 206 mg, sodium 3 mg store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F) avoid excessive heat see end flap for expiration date and lot number

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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 gout diabetes 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 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.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API