CYTRA-K CRYSTALS (Potassium Citrate and Citric Acid for Oral Solution)

Manufacturer
Cypress Pharmaceutical, Inc. | Tower Laboratories Ltd
Effective date
2016-09-20
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 20:22:52

Label at a glance#

ProductCytra-K Crystals
Active ingredientPotassium Citrate, Citric Acid Monohydrate
Label structure14 sections

Indications and uses

CYTRA-K CRYSTALS is an effective alkalinizing agent useful in those conditions where long-term maintenance of an alkaline urine is desirable, such as in patients with uric acid and cystine calculi of the urinary tract, especially when the administration of sodium salts is undesirable or contraindicated. In addition, it is a valuable adjuvant when administered with uricosuric agents in gout therapy, since urates te...

Dosage and administration

CYTRA-K CRYSTALS should be taken mixed in cool water or juice according to directions, followed by additional water or juice, if desired. Proper dilution may help prevent gastroin-testinal injury associated with the oral ingestion of concentrated potassium salt preparations. CYTRA-K CRYSTALS - Contents of 1 packet reconstituted with at least 6 ounces of cool water or juice, after meals and at bedtime, or as direct...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Rx Only

NDC 60258-005-01

DESCRIPTION

DESCRIPTION SECTION

CYTRA-K CRYSTALS (potassium citrate and citric acid for oral solution) is a pleasant-tasting oral systemic alkalizer containing potassium citrate and citric acid in a sugar-free base.

Each packet of CYTRA-K CRYSTALS, when reconstituted, provides the following amounts of active ingredients :
Potassium Citrate Monohydrate3300 mg
Citric Acid Monohydrate1002 mg
and provides 30 mEq potassium, equivalent to 30 mEq bicarbonate (HCO3).

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sodium saccharin, fruit punch flavor, and FD&C Red Dye #3.

Potassium Citrate Monohydrate has the chemical name: 1,2,3-Propanetricarboxylic acid, 2-hydroxy-,tripotassium salt, monohydrate. Its chemical structure is as follows:

C6H5K3O7 ∙ H2O M.W. 324.41
C6H5K3O7 ∙ H2O M.W. 324.41

Citric Acid Monohydrate has the chemical name: 1,2,3-Propanetricarboxylic acid, 2-hydroxy-, monohydrate. Its chemical structure is as follows:

C6H8O7 ∙ H2O M.W. 210.14
C6H8O7 ∙ H2O M.W. 210.14

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Potassium citrate is absorbed and metabolized to potassium bicarbonate, thus acting as a systemic alkalizer. The effects are essentially those of chlorides before absorption and those of bicarbonates subsequently. Oxidation is virtually complete so that less than 5% of the potassium citrate is excreted in the urine unchanged.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

CYTRA-K CRYSTALS is an effective alkalinizing agent useful in those conditions where long-term maintenance of an alkaline urine is desirable, such as in patients with uric acid and cystine calculi of the urinary tract, especially when the administration of sodium salts is undesirable or contraindicated. In addition, it is a valuable adjuvant when administered with uricosuric agents in gout therapy, since urates tend to crystallize out of an acid urine. It is also effective in correcting the acidosis of certain renal tubular disorders where the administration of potassium citrate may be preferable. CYTRA-K CRYSTALS is highly concentrated, and when administered after meals and before bedtime, allows one to maintain an alkaline urinary pH around the clock, usually without the necessity of a 2 A.M. dose. CYTRA-K CRYSTALS alkalinizes the urine without producing a systemic alkalosis in recommended dosage. It is highly palatable, pleasant tasting, and tolerable, even when administered for long periods. Potassium citrate does not neutralize the gastric juice or disturb digestion.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Severe renal impairment with oliguria or azotemia, untreated Addison's disease, adynamia episodica hereditaria, acute dehydration, heat cramps, anuria, severe myocardial damage, and hyperkalemia from any cause. Known hypersensitivity to any ingredients in this product.

WARNINGS AND PRECAUTIONS

WARNINGS SECTION

There have been several reports, published and unpublished, concerning nonspecific small-bowel lesions consisting of stenosis, with or without ulceration, associated with the administration of enteric-coated thiazides with potassium salts. These lesions may occur with enteric-coated potassium tablets alone or when they are used with nonenteric-coated thiazides, or certain other oral diuretics. These small-bowel lesions have caused obstruction, hemorrhage, and perforation. Surgery was frequently required and deaths have occurred. Based on a large survey of physicians and hospitals, both United States and foreign, the incidence of these lesions is low, and a causal relationship in man has not been definitely established. Available information tends to implicate enteric-coated potassium salts, although lesions of this type also occur spontaneously. Therefore, coated potassium-containing formulations should be administered only when indicated, and should be discontinued immediately if abdominal pain, distention, nausea, vomiting, or gastrointestinal bleeding occur. Large doses may cause hyperkalemia and alkalosis, especially in the presence of renal disease. Concurrent administration of potassium-containing medication, potassium-sparing diuretics, angiotensin-converting enzyme (ACE) inhibitors, or cardiac glycosides may lead to toxicity. Do not exceed recommended dosage. Discontinue use if adverse reactions occur.

Should be used with caution by patients with low urinary output unless under the supervision of a physician. As with all liquids containing a high concentration of potassium, patients should be directed to dilute adequately with water to minimize the possibility of gastrointestinal injury associated with the oral ingestion of concentrated potassium salt preparations; and preferably, to take each dose after meals to avoid saline laxative effect.

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

CYTRA-K CRYSTALS is generally well tolerated without any unpleasant side effects when given in recommended doses to patients with normal renal function and urinary output. However, as with any alkalinizing agent, caution must be used in certain patients with abnormal renal mechanisms to avoid development of hyperkalemia or alkalosis. Potassium intoxication causes listlessness, weakness, mental confusion, tingling of extremities, and other symptoms associated with a high concentration of potassium in the serum. Periodic determinations of serum electrolytes should be carried out in those patients with renal disease in order to avoid these complications. Hyperkalemia may exhibit the following electrocardiographic abnormalities: Disappearance of the P wave, widening and slurring of QRS complex, changes of the S-T segment, tall peaked T waves, etc.

OVERDOSAGE

OVERDOSAGE SECTION

The administration of oral potassium salts to persons with normal excretory mechanisms for potassium rarely causes serious hyperkalemia. However, if excretory mechanisms are impaired, hyperkalemia can result (see Contraindications and Warnings). Hyperkalemia, when detected, must be treated immediately because lethal levels can be reached in a few hours.

Treatment

SPL UNCLASSIFIED SECTION

Should hyperkalemia occur, treatment measures include the following:

(1) Elimination of foods or medications containing potassium. (2) The intravenous administration of 300 to 500 mL/hr of dextrose solution (10 to 25%), containing 10 units of insulin /20 gm dextrose. (3) The use of exchange resins, hemodialysis, or peritoneal dialysis. In treating hyperkalemia, it should be recalled that in patients who have been stabilized on digitalis, too rapid a lowering of the plasma potassium concentration can produce digitalis toxicity.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

CYTRA-K CRYSTALS should be taken mixed in cool water or juice according to directions, followed by additional water or juice, if desired. Proper dilution may help prevent gastroin-testinal injury associated with the oral ingestion of concentrated potassium salt preparations.

Usual Adult Dose

SPL UNCLASSIFIED SECTION

CYTRA-K CRYSTALS - Contents of 1 packet reconstituted with at least 6 ounces of cool water or juice, after meals and at bedtime, or as directed by physician.

Usual Pediatric Dose

SPL UNCLASSIFIED SECTION

CYTRA-K CRYSTALS is not recommended for pediatric use.

Usual Dosage Range

SPL UNCLASSIFIED SECTION

Contents of 1 packet CYTRA-K CRYSTALS, reconstituted as directed and taken four times a day, will usually maintain a urinary pH of 6.5-7.4. To check urinary pH, HYDRION Paper (pH 6.0-8.0) or NITRAZINE Paper (pH 4.5-7.5) are available and easy to use.

HOW SUPPLIED

HOW SUPPLIED SECTION

CYTRA-K CRYSTALS - 100 Packets/box (NDC 60258-005-01).

STORAGE

STORAGE AND HANDLING SECTION

Store at controlled room temperature, 15°-30°C (59°-86°F). Protect from excessive heat or freezing.

SPL UNCLASSIFIED SECTION

KEEP THIS PRODUCT OUT OF THE REACH OF CHILDREN. IN CASE OF ACCIDENTAL OVERDOSAGE, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

Call your doctor for medical advice about side effects. You may report side effects to Cypress Pharmaceutical, Inc. at 1-800-793-2145 or FDA at 1-800-FDA-1088.

SPL UNCLASSIFIED SECTION

Rx Only

Manufactured for: Cypress Pharmaceutical, Inc., Morristown, NJ 07960

I185
PN 0654C
Rev. 09/16

PRINCIPAL DISPLAY PANEL - 4.32 g Packet Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 60258-005-01

CYTRA-K CRYSTALS
(POTASSIUM CITRATE AND CITRIC ACID FOR ORAL SOLUTION)

FRUIT-FLAVORED • SUGAR-FREE

CYPRESS
PHARMACEUTICAL, INC.

100 Packets - Net weight per packet: 4.32 g

PRINCIPAL DISPLAY PANEL - 4.32 g Packet Box
PRINCIPAL DISPLAY PANEL - 4.32 g Packet Box

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1652638CYTRA-K CRYSTALS 3300 MG / 1002 MG Powder for Oral SolutionPSN3
1652634potassium citrate 3300 MG / citric acid 1002 MG Powder for Oral SolutionPSN3
1652638citric acid 1002 MG / potassium citrate 3300 MG Powder for Oral Solution [Cytra-K]SBD3
1652634citric acid 1002 MG / potassium citrate 3300 MG Powder for Oral SolutionSCD3
1652634Citric Acid 1002 MG / K+ citrate 3300 MG Powder for Oral SolutionSY3
1652638Citric Acid 1002 MG / K+ citrate 3300 MG Powder for Oral Solution [Cytra-K]SY3
1652634Citric Acid 1002 MG / Pot citrate 3300 MG Powder for Oral SolutionSY3
1652638Citric Acid 1002 MG / Pot citrate 3300 MG Powder for Oral Solution [Cytra-K]SY3
1652638Cytra-K (citric acid 1002 MG / potassium citrate 3300 MG) Powder for Oral SolutionSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ANHYDROUS CITRIC ACID Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60258-005-012020-01-31C16284748780-19d75b9cf-ea98-f424-e053-dadaa90a57ceCYTRA-K CRYSTALS (Potassium Citrate and Citric Acid for Oral Solution)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60258-005-01Cytra-K Crystals100 in 1 BOXGRANULE, FOR SOLUTION1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60258-005CYTRA-K CRYSTALS (POTASSIUM CITRATE AND CITRIC ACID ) GRANULE, FOR SOLUTION [CYPRESS PHARMACEUTICAL, INC.]3Legacy NDC, 1 package rows20160921_490c77d7-47f8-439f-aa37-953692f4c23a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60258-005-01EA - Each60258-005e30a9ee3-1186-4875-9b4b-714ca8733c4312012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Citric Acid MonohydrateACTIVE INGREDIENT2968PHW8QP1
Potassium CitrateACTIVE INGREDIENTEE90ONI6FF1
Citric AcidACTIVE MOIETY2968PHW8QP1
Potassium CationACTIVE MOIETY295O53K1521
Saccharin Sodium AnhydrousINACTIVE INGREDIENTI4807BK6021

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60258-00560258-005-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 17 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602LIQUID / ORAL1.5 mg/5mlExact identifier — unii candidate
17 equally ranked IID candidates
Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602PASTE, DENTIFRICE / DENTAL0.15 %w/wExact identifier — unii candidate
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Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602SOLUTION / ORAL20 mgExact identifier — unii candidate
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Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602TABLET, CHEWABLE / ORAL7.5 mgExact identifier — unii candidate
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Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602MOUTHWASH / BUCCAL0.2 mg/1mlExact identifier — unii candidate
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Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602WAFER / ORAL4.8 mgExact identifier — unii candidate
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Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602INJECTION / INTRAVENOUS0.09 %w/vExact identifier — unii candidate
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Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602EMULSION / ORAL0.4 mg/1mlExact identifier — unii candidate
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Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602SUSPENSION / ORAL16.65 mg/5mlExact identifier — unii candidate
17 equally ranked IID candidates
Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602TABLET, FILM COATED / ORAL0.35 mgExact identifier — unii candidate
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Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602SOLUTION / NASAL0.5 mg/1mlExact identifier — unii candidate
17 equally ranked IID candidates
Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602TABLET / ORAL97 mgExact identifier — unii candidate
17 equally ranked IID candidates
Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602DROPS / NASAL0.5 mg/1mlExact identifier — unii candidate
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Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602SYRUP / ORAL3.96 mg/5mlExact identifier — unii candidate
17 equally ranked IID candidates
Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602INJECTION / INTRAMUSCULAR0.09 %w/vExact identifier — unii candidate
17 equally ranked IID candidates
Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602POWDER, FOR SUSPENSION / ORAL18.75 mg/5mlExact identifier — unii candidate
17 equally ranked IID candidates
Saccharin Sodium AnhydrousSACCHARIN SODIUM ANHYDROUSI4807BK602SOLUTION / RECTAL0.67 %w/vExact identifier — unii candidate
17 equally ranked IID candidates

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
9625f8fc-b958-4054-9580-826d15156ba5490c77d7-47f8-439f-aa37-953692f4c23a2016-09-20Warnings, Adverse reactionsExact identifier
spl id: 9625f8fc-b958-4054-9580-826d15156ba5
spl set id: 490c77d7-47f8-439f-aa37-953692f4c23a

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