LIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH- acetaminophen tablet

Lil Drug Store Pain Reliever by

Drug Labeling and Warnings

Lil Drug Store Pain Reliever by is a Otc medication manufactured, distributed, or labeled by Lil' Drug Store Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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  • SPL UNCLASSIFIED SECTION

    Product distributed by:
    Lil' Drug Store Products, Inc.
    9300 Earhart Lane SW
    Cedar Rapids, IA 52404

  • PRINCIPAL DISPLAY PANEL - 500 mg Caplet Bottle Carton - NDC: 66715-6817-4

    QUALITY
    GUARANTEED

    Compare to the
    Active Ingredient in
    Tylenol® Extra Strength**

    Extra Strength

    Pain Reliever

    Acetaminophen

    Pain Reliever/Fever Reducer, 500 mg

    ACTUAL SIZE

    24
    Caplets

    Lil'
    Drug Store®

    PRINCIPAL DISPLAY PANEL - 500 mg Caplet Bottle Carton - NDC: <a href=/NDC/66715-6817-4>66715-6817-4</a>
  • PRINCIPAL DISPLAY PANEL - 500 mg Caplet Bottle Carton - NDC: 66715-6827-4

    QUALITY
    GUARANTEED

    Compare to the
    Active Ingredient in
    Tylenol® Extra Strength**

    Extra Strength

    Pain Reliever

    Acetaminophen

    Pain Reliever/Fever Reducer, 500 mg

    ACTUAL SIZE

    24
    Caplets

    Lil'
    Drug Store®

    PRINCIPAL DISPLAY PANEL - 500 mg Caplet Bottle Carton - NDC: <a href=/NDC/66715-6827-4>66715-6827-4</a>
  • PRINCIPAL DISPLAY PANEL - 500 mg Caplet Bottle Carton - NDC: 66715-6837-4

    QUALITY
    GUARANTEED

    Compare to the
    Active Ingredient in
    Tylenol® Extra Strength**

    Extra Strength

    Pain Reliever

    Acetaminophen

    Pain Reliever/Fever Reducer, 500 mg

    ACTUAL SIZE

    24
    Caplets

    Lil'
    Drug Store®

    PRINCIPAL DISPLAY PANEL - 500 mg Caplet Bottle Carton - NDC: <a href=/NDC/66715-6837-4>66715-6837-4</a>
  • INGREDIENTS AND APPEARANCE
    LIL DRUG STORE PAIN RELIEVER   EXTRA STRENGTH
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66715-6817
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen500 mg
    Inactive Ingredients
    Ingredient NameStrength
    Starch, Corn (UNII: O8232NY3SJ)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Lactose Monohydrate (UNII: EWQ57Q8I5X)  
    Magnesium Stearate (UNII: 70097M6I30)  
    Maltodextrin (UNII: 7CVR7L4A2D)  
    Medium-Chain Triglycerides (UNII: C9H2L21V7U)  
    Mineral Oil (UNII: T5L8T28FGP)  
    Polydextrose (UNII: VH2XOU12IE)  
    Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
    Polyvinyl Alcohol, Unspecified (UNII: 532B59J990)  
    Povidone, Unspecified (UNII: FZ989GH94E)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    Stearic Acid (UNII: 4ELV7Z65AP)  
    Talc (UNII: 7SEV7J4R1U)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize18mm
    FlavorImprint Code P500
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 66715-6817-41 in 1 CARTON04/15/2019
    124 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart34301/10/2015
    LIL DRUG STORE PAIN RELIEVER   EXTRA STRENGTH
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66715-6827
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen500 mg
    Inactive Ingredients
    Ingredient NameStrength
    Starch, Corn (UNII: O8232NY3SJ)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Lactose Monohydrate (UNII: EWQ57Q8I5X)  
    Magnesium Stearate (UNII: 70097M6I30)  
    Maltodextrin (UNII: 7CVR7L4A2D)  
    Medium-Chain Triglycerides (UNII: C9H2L21V7U)  
    Mineral Oil (UNII: T5L8T28FGP)  
    Polydextrose (UNII: VH2XOU12IE)  
    Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
    Polyvinyl Alcohol, Unspecified (UNII: 532B59J990)  
    Povidone, Unspecified (UNII: FZ989GH94E)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    Stearic Acid (UNII: 4ELV7Z65AP)  
    Talc (UNII: 7SEV7J4R1U)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize18mm
    FlavorImprint Code AV;0821
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 66715-6827-41 in 1 CARTON04/15/2019
    124 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart34301/10/2015
    LIL DRUG STORE PAIN RELIEVER   EXTRA STRENGTH
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66715-6837
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen500 mg
    Inactive Ingredients
    Ingredient NameStrength
    Starch, Corn (UNII: O8232NY3SJ)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Lactose Monohydrate (UNII: EWQ57Q8I5X)  
    Magnesium Stearate (UNII: 70097M6I30)  
    Maltodextrin (UNII: 7CVR7L4A2D)  
    Medium-Chain Triglycerides (UNII: C9H2L21V7U)  
    Mineral Oil (UNII: T5L8T28FGP)  
    Polydextrose (UNII: VH2XOU12IE)  
    Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
    Polyvinyl Alcohol, Unspecified (UNII: 532B59J990)  
    Povidone, Unspecified (UNII: FZ989GH94E)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    Stearic Acid (UNII: 4ELV7Z65AP)  
    Talc (UNII: 7SEV7J4R1U)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize18mm
    FlavorImprint Code TCL;341
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 66715-6837-41 in 1 CARTON04/15/2019
    124 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart34301/10/2015
    Labeler - Lil' Drug Store Products, Inc. (093103646)

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