Label: CONRX ALERT- caffeine tablet

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 11, 2013

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each caplet)

    Caffeine 200 mg

  • Purpose

    Alertness aid

  • Use

    helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness
  • Warnings

    For occasional use only

    Caffeine warning

    The recommended dose of this product contains about as much coffeube as a cup of coffee. Limit the use of caffeine-containing medications, foods, or beverages while taking this product because too much caffeine may cause nervousness, irritability, sleeplessness, and, occasionally, rapid heart beat.

    Do not use

    in children under 12 years of age
    as substitue for sleep

    Stop use and ask a doctor if fatigue or drowsiness persists or continues to recur

    If pregnant or breast-feeding, ask a health professional before use.

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

  • Directions

    adults and children 12 years of age and over: take ½ to 1 caplet not more often than every 3 to 4 hours
  • Other information

    store at room temperature
  • Inactive ingredients

    benzoic acid, carnauba wax, corn starch, FD&C blue # 1, hypromellose, light mineral oil, microcrystalline cellulose, polysorbate 20, povidone, propylene glycol, simethicone emulsion, sorbitan monolaurate, stearic acid, sucrose,titanium dioxide.

  • Question or comments?

    1-800-570-8650

  • PRINCIPAL DISPLAY PANEL - 50 Pouch Box

    Compare to the Active Ingredients in
    NoDoz

    MAXIMUM STRENGTH
    ConRx™

    Alert
    ALERTNESS AID

    TO OPEN
    PUSH IN TAB AND PULL OUT

    Compare to the Active Ingredients in
    NoDoz

    50 Pouches of 2 Caplets Each

    Principal Display Panel - 50 Pouch Box
  • INGREDIENTS AND APPEARANCE
    CONRX ALERT 
    caffeine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68737-229
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Caffeine (UNII: 3G6A5W338E) (Caffeine - UNII:3G6A5W338E) Caffeine200 mg
    Inactive Ingredients
    Ingredient NameStrength
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    POVIDONES (UNII: FZ989GH94E)  
    POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SUCROSE (UNII: C151H8M554)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorBLUEScore2 pieces
    ShapeOVALSize11mm
    FlavorImprint Code CRX
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68737-229-1350 in 1 BOX
    12 in 1 POUCH
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34002/15/2013
    Labeler - Eagle Distributors,Inc. (929837425)