NAUZENE (SODIUM CITRATE) SYRUP [ALVA-AMCO PHARMACAL COMPANIES, INC.]

NAUZENE (SODIUM CITRATE) SYRUP [ALVA-AMCO PHARMACAL COMPANIES, INC.]
PDF | XML

NDC 52389-172-04
Set ID 728376f5-6cab-404e-b519-f6c595291d6f
Category HUMAN OTC DRUG LABEL
Packager Alva-Amco Pharmacal Companies, Inc.
Generic Name
Product Class Anti-coagulant
Product Number
Application Number PART357
  • Active ingredients (in each 15-mL tablespoon)

    Dextrose (glucose) 4.35 g...........................anti-nausea

    Levulose (fructose) 4.17 g...........................anti-nausea

    Sodium citrate dihydrate, 0.921 g................antacid

  • Uses

    For the relief of nausea associated with upset stomach, including that due to overindulgence in food or drink.

  • Warnings


  • DO NOT USE

    Do not use if you have Hereditary Fructose Intolerance (HFI).  This product contains fructose.

  • Ask a doctor before use if you

    • you have diabetes because this product contains sugar
    • are on a sodium-restricted diet.
  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if you are taking any other medications.  Antacids may interact with certain prescription drugs.

  • WHEN USING

    When using this product do not take more than 6 does in a 24-hour period.

  • STOP USE

    Stop use and ask a doctor if nausea lasts more than two weeks or recurs frequently.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breastfeeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    • Read all package directions and warnings before use and use only as directed.
    • Adults:  1 - 2 tablespoons (15 - 30 mL).
    • Children:  Consult a doctor for appropriate dosage.
    • Dosage may be repeated after 30 minutes not to exceed 6 doses in a 24-hour period unless advised by a doctor.
    • For maximum effectiveness never dilute Nauzene or drink fluids of any kind immediately before or after taking Nauzene.
    • Nauzene Liquid is intended for use by normally healthy persons only.
    • Persons under 18 years of age should use only as directed by a doctor.
  • Other information

    • Sodium content 193 mg/tablespoon (15 mL).
    • Store at room temperature.
    • ** Contents sealed:  Each bottle of Nauzene Liquid has a tamper evident seal around the cap and a safety seal under the cap.  Do not use if either of these seals appears broken.  NOTE:  Nauzene is not intended as a substitute for a balanced nutritional diet or as an electrolyte replenishment.
    • Serious side effects associated with the use of this product may be reported to the phone number provided below.
  • Inactive ingredients

    Corn syrup, FDC Red No. 40 lake, flavor, fructose syrup, glycerin, methylparaben, phosphoric acid, purified water.

  • QUESTIONS

    Questions? 1-800-792-2582

  • PRINCIPAL DISPLAY PANEL

    Nauzene Liquid PDP

  • INGREDIENTS AND APPEARANCE
    NAUZENE 
    sodium citrate syrup
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52389-172
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) TRISODIUM CITRATE DIHYDRATE.921 g  in 15 mL
    Dextrose (UNII: IY9XDZ35W2) (Dextrose - UNII:IY9XDZ35W2) Dextrose4.35 g  in 15 mL
    Fructose (UNII: 6YSS42VSEV) (Fructose - UNII:6YSS42VSEV) Fructose4.17 g  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    corn syrup (UNII: 9G5L16BK6N)  
    FD&C Red No. 40 (UNII: WZB9127XOA)  
    High fructose corn syrup (UNII: XY6UN3QB6S)  
    Glycerin (UNII: PDC6A3C0OX)  
    Methylparaben (UNII: A2I8C7HI9T)  
    Phosphoric acid (UNII: E4GA8884NN)  
    Water (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorCHERRY (flavor) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52389-172-04118 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35702/15/2000
    Labeler - Alva-Amco Pharmacal Companies, Inc. (042074856)

Related Drugs