Label: QUALITY CHOICE NAUSEA RELIEF- sodium citrate dihydrate tablet, chewable

  • NDC Code(s): 83324-300-42
  • Packager: QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 1, 2025

If you are a consumer or patient please visit this version.

  • Active ingredient (in each chewable tablet)

    Sodium citrate dihydrate 230 mg

  • Purpose

    Upset stomach reliever

  • Uses

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

  • Warnings

  • DO NOT USE

    Do not useif you

    • have Hereditary Fructose Intolerance (HFI).  This product contains fructose.
  • Ask a doctor before use if 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 aretaking any other medications. This product may interact with certain prescription drugs.

  • WHEN USING

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

  • STOP USE

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

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding,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 at 1-800-222-1222.

  • Directions

    • Adults: 2-4 tablets.
    • Children: Consult a doctor for appropriate dosage.
    • Chew tablets completely. Do not swallow tablet whole.
    • Dosage may be repeated after 15 minutes, not to exceed 24 tablets in a 24-hour period unless advised by a doctor.
    • Read all package directions and warnings before use and use only as directed.
    • These tablets are intended for use by normally healthy persons only.
    • Persons under 18 years of age should use only as directed by a doctor.
  • Other information

    • Each tablet contains:sodium 60 mg
    • Store at room temperature.
    • Protect product from excessive heat, cold and moisture.
    • Note:  This product is not intended as a substitute for a balanced nutritional diet or as an electrolyte replenishment.
    • You may report serious side effects to the phone number provided under Questions?
  • Inactive ingredients

    dextrose, FDC Red No. 40, flavors, fructose, hydroxypropyl cellulose, magnesium stearate, maltodextrin, silica, sodium carboxymethylcellulose, sucralose.

  • Questions

    1-866-467-2748

  • Principal Display Panel

    Quality Choice®

    *Compare to the Active Ingredient in Nauzene® Tablets

    NDC# 83324-300-42

    Nausea Relief

    For upset stomach & nausea

    With electrolyte**

    Free From:

    Gluten, Aspartame

    Aspirin and Salicylate

    Wild Cherry Flavor

    Naturally & Artificially Flavored

    42 CHEWABLE TABLETS

    TAMPER EVIDENT: DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING

    IMPORTANT: Keep this carton for future reference on full labeling

    Distributed by: CDMA, Inc.

    Novi, MI 48375

    Questions: 800-935-2362

    100% SATISFACTION GUARANTEED

    *This product is not manufactured of distributed by ALVA-AMCO Pharmacal Cos., Inc., the distributor of Nauzene® Tablets.

    **Sodium citrate dihydrate

    Quality Choice Nausea Relief 42 Chewable Tablets
  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE   NAUSEA RELIEF
    sodium citrate dihydrate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-300
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID230 mg
    Inactive Ingredients
    Ingredient NameStrength
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    CHERRY (UNII: BUC5I9595W)  
    FRUCTOSE (UNII: 6YSS42VSEV)  
    HYDROXYPROPYL CELLULOSE (110000 WAMW) (UNII: 5Y0974F5PW)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorpinkScoreno score
    ShapeROUNDSize16mm
    FlavorCHERRY (Wild Cherry Flavor) Imprint Code RP183
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83324-300-423 in 1 CARTON09/15/2025
    114 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/15/2025
    Labeler - QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) (011920774)