Oracit

Carolina Medical Products Company

ORACITOral Citrate (Shohl’s Solution)

FULL PRESCRIBING INFORMATION: CONTENTS*

• ORACIT DESCRIPTION
• ACTION
• INDICATIONS
• ORACIT CONTRAINDICATIONS
• PRECAUTIONS
• ORACIT ADVERSE REACTIONS
• ORACIT DOSAGE AND ADMINISTRATION
• HOW SUPPLIED
• PACKAGE/LABEL PRINCIPAL DISPLAY PANEL - BOTTLE LABEL

FULL PRESCRIBING INFORMATION

ORACIT DESCRIPTION

The product is a clear, colorless solution containing Citric Acid USP 640 mg/5 mL, and Hydrous Sodium Citrate USP 490 mg/5 mL. It also contains Methylparaben NF and Propylparaben NF as preservatives. These concentrations yield 1 mEq of sodium, equivalent to 1 mEq of bicarbonate per mL of solution.

ACTION

Oral citrate solution is used as a systemic and urinary alkalinizer. Less than 5% of the citrate is excreted in the urine unchanged, since citrate oxidation is to a great extent complete.

INDICATIONS

ORACIT^® is indicated for the treatment of metabolic acidosis. This solution is also useful in conditions where long term maintenance of alkaline urine is needed (e.g. uric acid and cystine calculi of the urinary tract). ORACIT^® is also effective in treatment for acidosis of certain renal tubular disorders.

ORACIT CONTRAINDICATIONS

ORACIT^® is contraindicated in patients with severe renal impairment, oliguria or azotemia, untreated Addison’s disease, adynamia episodica hereditaria, acute dehydration, heat cramp, anuria, severe myocardial damage, and hyperkalemia.

PRECAUTIONS

The citrate solution should be used with caution in patients with impaired renal function to avoid hypernatremia or alkalosis in the presence of hypocalcemia. Periodic determinations of serum electrolyte levels (especially bicarbonate levels) should be done in patients with renal disease to avoid cardiac failure, hypertension, peripheral and pulmonary edema, and toxemia of pregnancy. The solution should be diluted with water and preferably taken after meals to avoid saline laxative effects.

ORACIT ADVERSE REACTIONS

Citrate solution is generally well tolerated when given in recommended doses when the patient has normal renal functions.

ORACIT DOSAGE AND ADMINISTRATION

The dose of ORACIT^® is 10 to 30 mL, diluted with water, after meals and at bedtime. The dose should be titrated to achieve desired effects.

HOW SUPPLIED

ORACIT^® is supplied in 500 mL bottles (NDC 46287-014-01), 30 mL unit dose bottles, 10 bottles per carton (NDC 46287-014-30), and 15 mL unit dose bottles, 10 bottles per carton (NDC 46287-014-15).

Dispense in well-closed containers.

STORE AT CONTROLLED ROOM TEMPERATURE (15° - 30° C)

Carolina Medical Products Co.

Post Office Box 147

Farmville, North Carolina 27828

Revised May 1986

Copyright ^© Carolina Medical Products Co. 1985

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL - BOTTLE LABEL

NDC 48287-014-01

500 mL

ORACIT^®

ORAL CITRATE (SHOHL'S) SOLUTION

Contains: Hydrous Sodium Citrate USP 490 mg/5mL; Citric Acid USP 640 mg/5mL; Methylparaben NF; Propylparaben NF; Alcohol 0.25%

CAUTION: Federal law prohibits dispensing without prescription.

USUAL DOSAGE: See package insert.

DISPENSE IN A WELL-CLOSED CONTAINER.

STORE AT CONTROLLED ROOM TEMPERATURE 15° - 30° C (59° - 86° F).

BATCH:

EXP:

Carolina Medical Products Co.

Post Office Box 147

Farmville, North Carolina 27828