Label: CONRX ALERT- caffeine tablet 

  • Label RSS
  • NDC Code(s): 68737-229-13
  • Packager: Eagle Distributors,Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 02/13

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

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  • Active ingredient (in each caplet)

    Caffeine 200 mg

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  • Purpose

    Alertness aid

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  • Use

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

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  • Directions

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

    store at room temperature
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  • 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.

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  • Question or comments?

    1-800-570-8650

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  • 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
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  • INGREDIENTS AND APPEARANCE
    CONRX ALERT 
    caffeine tablet
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:68737-229
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Caffeine (Caffeine) Caffeine 200 mg
    Inactive Ingredients
    Ingredient Name Strength
    BENZOIC ACID  
    CARNAUBA WAX  
    STARCH, CORN  
    FD&C BLUE NO. 1  
    HYPROMELLOSES  
    LIGHT MINERAL OIL  
    CELLULOSE, MICROCRYSTALLINE  
    POLYSORBATE 20  
    POVIDONES  
    POLYETHYLENE GLYCOL 6000  
    DIMETHICONE  
    SORBITAN MONOLAURATE  
    STEARIC ACID  
    SUCROSE  
    TITANIUM DIOXIDE  
    Product Characteristics
    Color BLUE Score 2 pieces
    Shape OVAL Size 11mm
    Flavor Imprint Code CRX
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68737-229-13 50 in 1 BOX
    1 2 in 1 POUCH
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part340 02/15/2013
    Labeler - Eagle Distributors,Inc. (929837425)
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