Label: CIRCLE K NOSNOOZE- caffeine tablet

  • NDC Code(s): 66715-5730-2
  • Packager: Lil' Drug Store Products, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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 September 26, 2019

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each tablet)

    Caffeine 200mg

  • 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 caffeine 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 substitute 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 oldertake 1 tablet (200 mg) not more often than every 3 to 4 hours
    children under 12 years of agedo not use
  • Other information

    • store at room temperature
    • avoid excessive heat (greater than 100°F) and humidity
    • do not use if inner pouch or carton is open or damaged
    • see bottom panel for lot number and expiration date
  • Inactive ingredients

    croscarmellose sodium1, colloidal silicon dioxide1, D&C yellow #101, dicalcium phosphate dihydrate1, FD&C blue #11, FD&C yellow #61, hypromellose1, magnesium stearate, microcrystalline cellulose, povidone1, propylene glycol1, sodium starch glycolate1, sucrose1, titanium dioxide1, triacetin1.


    1
    may contain
  • Questions or comments?

    call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST)

  • SPL UNCLASSIFIED SECTION

    Proudly distributed by Circle K Stores Inc.

  • PRINCIPAL DISPLAY PANEL - 200 mg Tablet Pouch Carton

    K®

    NoSnooze
    Alertness Aid, Caffeine 200 mg

    Maximum Strength

    -
    Fast & Effective
    -
    Safe as Coffee

    4 Tablets

    2 POUCHES, 2 TABLETS PER POUCH

    Principal Display Panel - 200 mg Tablet Pouch Carton
  • INGREDIENTS AND APPEARANCE
    CIRCLE K NOSNOOZE 
    caffeine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-5730
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Caffeine (UNII: 3G6A5W338E) (Caffeine - UNII:3G6A5W338E) Caffeine200 mg
    Inactive Ingredients
    Ingredient NameStrength
    Croscarmellose Sodium (UNII: M28OL1HH48)  
    Silicon Dioxide (UNII: ETJ7Z6XBU4)  
    D&C yellow No. 10 (UNII: 35SW5USQ3G)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    FD&C blue No. 1 (UNII: H3R47K3TBD)  
    FD&C yellow No. 6 (UNII: H77VEI93A8)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Magnesium Stearate (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Sodium Starch Glycolate Type A Corn (UNII: AG9B65PV6B)  
    Sucrose (UNII: C151H8M554)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Triacetin (UNII: XHX3C3X673)  
    Sodium Starch Glycolate Type A Potato (UNII: 5856J3G2A2)  
    Product Characteristics
    ColorYELLOWScoreno score
    ShapeROUNDSize11mm
    FlavorImprint Code 212;212
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-5730-22 in 1 CARTON11/01/201409/25/2022
    12 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34011/01/201409/25/2022
    Labeler - Lil' Drug Store Products, Inc (093103646)