SODIUM CITRATE AND CITRIC ACID (SODIUM CITRATE AND CITRIC ACID MONOHYDRATE) SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]

SODIUM CITRATE AND CITRIC ACID (SODIUM CITRATE AND CITRIC ACID MONOHYDRATE) SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]
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NDC 0121-0595-00, 0121-0595-15, 0121-0595-16, 0121-0595-30, 0121-1190-00, 0121-1190-30
Set ID 63201a61-6ac5-41ae-8b2d-ff0d3a8ddfd5
Category HUMAN PRESCRIPTION DRUG LABEL
Packager Pharmaceutical Associates, Inc.
Generic Name
Product Class Anti-coagulant
Product Number
Application Number
  • SPL UNCLASSIFIED SECTION

    A Sugar-Free Systemic Alkalizer

  • DESCRIPTION

    Sodium Citrate and Citric Acid Oral Solution USP is a stable and pleasant-tasting systemic alkalizer containing sodium citrate and citric acid in a sugar-free base. It is a nonparticulate neutralizing buffer.

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

    SODIUM CITRATE Dihydrate 500 mg (0.34 Molar)
    CITRIC ACID Monohydrate 334 mg (0.32 Molar)

    Each mL contains 1 mEq sodium ion and is equivalent to 1 mEq bicarbonate (HCO3).

    INACTIVE INGREDIENTS: Flavoring, polyethylene glycol, propylene glycol, purified water, sodium benzoate, and sorbitol solution.

  • 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 USP 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 USP 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 USP 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 USP 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 USP 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, grape flavor) is supplied in the following oral dosage forms:

    NDC 0121-0595-16:  16 fl oz (473 mL) bottle

    NDC 0121-0595-15:  15 mL unit dose cup

    NDC 0121-0595-00:  Case contains 100 unit dose cups of 15 mL (0121-0595-15) packaged in 10 trays of 10 unit dose cups each.

    NDC 0121-1190-30:  30 mL unit dose cup

    NDC 0121-1190-00:   Case contains 100 unit dose cups of 30 mL (0121-1190-30) packaged in 10 trays of 10 unit dose cups each.

  • STORAGE:

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

  • SPL UNCLASSIFIED SECTION

    Rx ONLY

    Manufactured By:
    Pharmaceutical Associates, Inc.
    Greenville, SC 29605
    www.paipharma.com 

    R06/16

  • PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

    NDC 0121-0595-16
    NSN 6505-01-097-4766

    Sodium Citrate
    and Citric Acid
    Oral Solution USP

    500 mg/334 mg per 5 mL

    A SUGAR-FREE SYSTEMIC ALKALIZER

    Each teaspoonful (5 mL) contains:
    Sodium Citrate Dihydrate..........500 mg
    Citric Acid Monohydrate............334 mg
    Each mL provides 1 mEq Sodium Ion and is
    equivalent to 1 mEq Bicarbonate (HCO3).

    Rx ONLY

    16 fl oz (473 mL)

    pai
    Pharmaceutical
    Associates, Inc.

    Greenville, SC 29605

    DOSAGE AND ADMINISTRATION:
    Sodium Citrate and Citric Acid Oral
    Solution USP should be taken diluted in
    water followed by additional water, if 
    desired. SHAKE WELL BEFORE USING. 

    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.

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

    Dispense in a tight, light-resistant
    container with a child-resistant closure.

    INDICATIONS AND USAGE: Sodium
    Citrate and Citric Acid Oral Solution
    USP is a stable systemic alkalizer in
    a palatable sugar-free base. It is
    useful in the management of
    metabolic acidosis especially when
    the administration of potassium salts
    is undesirable or contraindicated.

    SEE ACCOMPANYING LITERATURE.

    473 mL Bottle Label

  • PRINCIPAL DISPLAY PANEL - 30 mL Unit Dose Cup Label

    Delivers 30 mL
    NDC 0121-1190-30

    S ODIUM C ITRATE and
    C ITRIC A CID O RAL
    S OLUTION USP (Sugar Free)

    3 g/2 g per 30 mL

    SHAKE WELL-DILUTE AS DIRECTED

    FOR INSTITUTIONAL USE ONLY

    Rx ONLYPHARMACEUTICAL ASSOCIATES, INC.
    GREENVILLE, SC 29605
    SEE INSERT

    F05953002

    30 mL Unit Dose Cup Label

  • PRINCIPAL DISPLAY PANEL - 15 mL Unit Dose Cup Label

    Delivers 15  mL
    NDC 0121-0595-15

    S ODIUM C ITRATE and
    C ITRIC A CID O RAL
    S OLUTION USP (sugar Free)

    1.5 g/1 g per 15 mL

    SHAKE WELL-DILUTE AS DIRECTED

    FOR INSTITUTIONAL USE ONLY

    Rx ONLYPHARMACEUTICAL ASSOCIATES, INC.
    GREENVILLE, SC 29605
    SEE INSERT

    F05951501

    15 mL Unit Dose Cup Label

  • INGREDIENTS AND APPEARANCE
    SODIUM CITRATE AND CITRIC ACID 
    sodium citrate and citric acid monohydrate solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0121-0595
    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
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID334 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorGRAPEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0121-0595-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/1969
    2NDC:0121-0595-0010 in 1 CASE01/01/1969
    210 in 1 TRAY
    2NDC:0121-0595-1515 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product
    3NDC:0121-0595-3010 in 1 CASE01/01/1969
    310 in 1 TRAY
    330 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/1969
    SODIUM CITRATE AND CITRIC ACID 
    sodium citrate and citric acid monohydrate solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0121-1190
    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
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID334 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorGRAPEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0121-1190-0010 in 1 CASE01/01/1969
    110 in 1 TRAY
    1NDC:0121-1190-3030 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/1969
    Labeler - Pharmaceutical Associates, Inc. (044940096)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharmaceutical Associates, Inc.097630693manufacture(0121-0595, 0121-1190)