Label: SODIUM CITRATE AND CITRIC ACID solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 5, 2023

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  • SPL UNCLASSIFIED SECTION

    A Sugar-Free Systemic Alkalizer

  • DESCRIPTION

    Sodium Citrate and Citric Acid Oral Solution, USP is a clear stable and cherry flavored systemic alkalizer containing sodium citrate and citric acid in a sugar-free base with cherry flavor. It is a nonparticulate neutralizing buffer.

    Sodium Citrate and Citric Acid Oral Solution USP contains in each teaspoonful (5 mL):

    Sodium Citrate Dihydrate, USP 500 mg (0.34 Molar)
    Citric Acid Monohydrate, USP 334 mg (0.32 Molar)

    Each mL contains 1 mEq sodium ion and is equivalent to 1 mEq bicarbonate (HCO 3).

    INACTIVE INGREDIENTS: purified water, saccharin sodium, sodium benzoate, sorbitol solution, and  wild cherry flavor.

  • CLINICAL PHARMACOLOGY

    Sodium citrate is absorbed and metabolized to sodium 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 sodium citrate is excreted in the urine unchanged.

  • INDICATIONS AND USAGE

    Sodium citrate and citric acid oral solution, is an effective alkalinizing agent. It is useful in those conditions where long-term maintenance of an alkaline urine is desirable, and is of value in the alleviation of chronic metabolic acidosis, such as results from chronic renal insufficiency or the syndrome of renal tubular acidosis, especially when the administration of potassium salts is undesirable or contraindicated. This product is also useful for buffering and neutralizing gastric hydrochloric acid quickly and effectively.

    Sodium citrate and citric acid oral solution is 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. This product alkalinizes the urine without producing a systemic alkalosis in the recommended dosage. This product is highly palatable, pleasant tasting, and tolerable, even when administered for long periods.

  • CONTRAINDICATIONS

    Patients on sodium-restricted diets or with severe renal impairment.

  • PRECAUTIONS

    Sodium citrate and citric acid oral solution should be used with caution by patients with low urinary output unless under the supervision of a physician. This product should not be administered concurrently with aluminum-based antacids. Patients should be directed to dilute adequately with water and preferably, to take each dose after meals to avoid saline laxative effect. Sodium salts should be used cautiously in patients with cardiac failure, hypertension, impaired renal function, peripheral and pulmonary edema, and toxemia of pregnancy. Periodic examinations and determinations of serum electrolytes, particularly serum bicarbonate level, should be carried out in those patients with renal disease in order to avoid these complications.

  • ADVERSE REACTIONS

    Sodium citrate and citric acid oral solution 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 alkalosis, especially in the presence of hypocalcemia.

  • OVERDOSAGE

    Overdosage with sodium salts may cause diarrhea, nausea and vomiting, hypernoia, and convulsions.

  • DOSAGE AND ADMINISTRATION

    Sodium citrate and citric acid oral solution should be taken diluted in water, followed by additional water, if desired. SHAKE WELL BEFORE USING.

    For Systemic Alkalization

    Usual Adult Dose

    2 to 6 teaspoonfuls (10 to 30 mL), diluted in 1 to 3 ounces of water, after meals and at bedtime, or as directed by a physician.

    Usual Pediatric Dose

    1 to 3 teaspoonfuls (5 to 15 mL), diluted in 1 to 3 ounces of water, after meals and at bedtime, or as directed by a physician. For children under two years of age, use is based on consultation with a physician.

    As a neutralizing buffer

    3 teaspoonfuls (15 mL), diluted with 15 mL water, taken as a single dose, or as directed by a physician.

  • HOW SUPPLIED

    Sodium Citrate and Citric Acid Oral Solution, USP (Colorless liquid with cherry flavor) is supplied in the following oral dosage form:

    NDC 62135-434-47:  473 mL (16 fl oz) bottle

    STORAGE:

    Keep tightly closed.  Store at controlled room temperature, 20°-25°C (68°-77°F).  Protect from freezing.

    Rx ONLY

    Manufactured for:
    Chartwell RX, LLC
    Congers, NY 10920

    L71144

    Rev. 12/2022

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL

    Sodium Citrate and Citric Acid Oral Solution, USP - NDC 62135-434-47 - 16 fl oz (473 mL) Bottle Label

    Sodium Citrate and Citric Acid Oral Solution, USP  - NDC 62135-434-47 - 16 fl oz (473 mL) Bottle Label
  • INGREDIENTS AND APPEARANCE
    SODIUM CITRATE AND CITRIC ACID 
    sodium citrate and citric acid solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:62135-434
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CITRATE (UNII: 1Q73Q2JULR) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) SODIUM CITRATE500 mg  in 5 mL
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID334 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL SOLUTION (UNII: 8KW3E207O2)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (clear) Score    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62135-434-47473 mL in 1 BOTTLE; Type 0: Not a Combination Product12/08/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/08/2022
    Labeler - Chartwell RX, LLC (079394054)
    Establishment
    NameAddressID/FEIBusiness Operations
    Chartwell Pharmaceuticals Carmel, LLC118673485analysis(62135-434) , manufacture(62135-434) , pack(62135-434)