Label: NODOZ ALERTNESS AID- caffeine tablet, film-coated tablet, film coated

  • NDC Code(s): 66715-9899-3, 66715-9899-4, 66715-9899-6
  • Packager: Lil' Drug Store Products, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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  • Drug Facts

  • Active ingredient

    Active ingredient (in each caplet)

    Caffeine 200 mg

  • Purpose

    Purpose

    Alertness aid

  • Use

    Use

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

    For occasional use only

    Caffeine warning

    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 heartbeat.

    Do not use

    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

    Directions

    • adults and children 12 years of age and over: take 1/2 to 1 caplet not more often than every 3 to 4 hours
    • children under 12 years: do not use
  • Other information

    Other information

    • store at 25°C (77°F); excursions permitted between 15°C-30°C (59°F-86°F)
    • see end flap for expiration date and lot number
    • use by expiration date on package
  • Inactive ingredients

    Inactive ingredients
    corn starch, dextrates hydrated, dibasic calcium phosphate dihydrate, flavor, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, stearic acid

  • Questions or comments?

    Questions or comments?

    call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST) or www.nodoz.com

  • PDP/Package 60ct

    Fights Fatigue • Max Strength

    NoDoz

    Aler tness Aid

    [caplet image]

    60 CAPLETS

    200 mg CAFFEINE EACH

    Carton

    Label

  • PDP/Package 6ct

    Fights Fatigue • Max Strength

    NoDoz

    Aler tness Aid

    [caplet image]

    200 mg CAFFEINE EACH

    6

    CAPLETS

    3POUCHES, 2 CAPLETS PER POUCH

    [Lil' Drug Store logo]

    PDP/Package 6ct

  • PDP/Package - 20 ct NDC 66715-9899-4

    Fights Fatigue • Max Strength

    NoDoz

    Alertness Aid

    [caplet image]

    20 CAPLETS

    200 mg CAFFEINE EACH

    PDP/Package

  • INGREDIENTS AND APPEARANCE
    NODOZ ALERTNESS AID 
    caffeine tablet, film-coated tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-9899
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE200 mg
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    DEXTRATES (UNII: G263MI44RU)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorwhiteScore2 pieces
    ShapeOVAL (capsule-shaped biconvex) Size15mm
    FlavorMINTImprint Code NoDoz
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-9899-61 in 1 CARTON01/02/2022
    160 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:66715-9899-33 in 1 CARTON05/24/2022
    22 in 1 POUCH; Type 0: Not a Combination Product
    3NDC:66715-9899-42 in 1 CARTON09/15/2022
    310 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01101/02/2022
    Labeler - Lil' Drug Store Products, Inc. (093103646)
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