COLD AND FLU DAYTIME- acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled COLD AND FLU DAYTIME- acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled

Cold and Flu Daytime by

Drug Labeling and Warnings

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

Drug Details [pdf]

  • Questions or comments?

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

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC: 66715-6831

    QUALITY
    ⋆ GUARANTEED ⋆

    Compare to the Active Ingredients in
    Vicks® DayQuil® LiquiCaps®**

    Non-drowsy

    Cold & Flu
    Daytime

    Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl
    Pain Reliever/Fever Reducer, Cough Suppressant, Nasal Decongestant

    Relieves

    • Aches Fever
    • Sore Throat Cough
    • Nasal Congestion

    ACTUAL SIZE

    12
    Softgels

    Lil'
    Drug Store®

    Principal Display Panel - 12 Softgel Blister Pack Carton - NDC: <a href=/NDC/66715-6831>66715-6831</a>
  • PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC: 66715-6851

    QUALITY
    ⋆ GUARANTEED ⋆

    Compare to the Active Ingredients in
    Vicks® DayQuil® LiquiCaps®**

    Non-drowsy

    Cold & Flu
    Daytime

    Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl
    Pain Reliever/Fever Reducer, Cough Suppressant, Nasal Decongestant

    Relieves

    • Aches Fever
    • Sore Throat Cough
    • Nasal Congestion

    ACTUAL SIZE

    12
    Softgels

    Lil'
    Drug Store®

    Principal Display Panel - 12 Softgel Blister Pack Carton - NDC: <a href=/NDC/66715-6851>66715-6851</a>
  • PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC: 66715-6951

    QUALITY
    ⋆ GUARANTEED ⋆

    Compare to the Active Ingredients in
    Vicks® DayQuil® LiquiCaps®**

    Non-drowsy

    Cold & Flu
    Daytime

    Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl
    Pain Reliever/Fever Reducer, Cough Suppressant, Nasal Decongestant

    Relieves

    • Aches Fever
    • Sore Throat Cough
    • Nasal Congestion

    ACTUAL SIZE

    12
    Softgels

    Lil'
    Drug Store®

    Principal Display Panel - 12 Softgel Blister Pack Carton - NDC: <a href=/NDC/66715-6951>66715-6951</a>
  • PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC: 66715-6852

    QUALITY
    ⋆ GUARANTEED ⋆

    Compare to the Active Ingredients in
    Vicks® DayQuil® LiquiCaps®**

    Cold & Flu
    Daytime

    Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl
    Pain Reliever/Fever Reducer, Cough Suppressant, Nasal Decongestant

    Relieves
    Aches Fever
    Sore Throat Cough
    Nasal Congestion

    ACTUAL SIZE

    12
    Softgels

    Lil'
    Drug Store®

    Principal Display Panel - 12 Softgel Blister Pack Carton - NDC: <a href=/NDC/66715-6852>66715-6852</a>
  • PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC: 66715-6853

    QUALITY
    ⋆ GUARANTEED ⋆

    Compare to the Active Ingredients in
    Vicks® DayQuil® LiquiCaps®**

    Cold & Flu
    Daytime

    Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl
    Pain Reliever/Fever Reducer, Cough Suppressant, Nasal Decongestant

    Relieves
    Aches Fever
    Sore Throat Cough
    Nasal Congestion

    ACTUAL SIZE

    12
    Softgels

    Lil'
    Drug Store®

    Principal Display Panel - 12 Softgel Blister Pack Carton - NDC: <a href=/NDC/66715-6853>66715-6853</a>
  • INGREDIENTS AND APPEARANCE
    COLD AND FLU DAYTIME 
    acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66715-6831
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen325 mg
    Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan Hydrobromide10 mg
    Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV) Phenylephrine Hydrochloride5 mg
    Inactive Ingredients
    Ingredient NameStrength
    Butylated Hydroxyanisole (UNII: REK4960K2U)  
    Butylated Hydroxytoluene (UNII: 1P9D0Z171K)  
    FD&C red No. 40 (UNII: WZB9127XOA)  
    FD&C yellow No. 6 (UNII: H77VEI93A8)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    Glycerin (UNII: PDC6A3C0OX)  
    Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
    Povidone, Unspecified (UNII: FZ989GH94E)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Sorbitan (UNII: 6O92ICV9RU)  
    Sorbitol (UNII: 506T60A25R)  
    Water (UNII: 059QF0KO0R)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorORANGEScoreno score
    ShapeOVALSize20mm
    FlavorImprint Code 95A
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 66715-6831-06 in 1 CARTON10/01/2015
    12 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34109/05/2014
    COLD AND FLU DAYTIME 
    acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66715-6851
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen325 mg
    Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan Hydrobromide10 mg
    Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV) Phenylephrine Hydrochloride5 mg
    Inactive Ingredients
    Ingredient NameStrength
    Butylated Hydroxyanisole (UNII: REK4960K2U)  
    Butylated Hydroxytoluene (UNII: 1P9D0Z171K)  
    FD&C red No. 40 (UNII: WZB9127XOA)  
    FD&C yellow No. 6 (UNII: H77VEI93A8)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    Glycerin (UNII: PDC6A3C0OX)  
    Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
    Povidone, Unspecified (UNII: FZ989GH94E)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Sorbitan (UNII: 6O92ICV9RU)  
    Sorbitol (UNII: 506T60A25R)  
    Water (UNII: 059QF0KO0R)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorORANGEScoreno score
    ShapeOVALSize20mm
    FlavorImprint Code P19
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 66715-6851-06 in 1 CARTON10/01/2015
    12 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34109/05/2014
    COLD AND FLU DAYTIME 
    acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66715-6951
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen325 mg
    Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan Hydrobromide10 mg
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
    Inactive Ingredients
    Ingredient NameStrength
    Butylated Hydroxyanisole (UNII: REK4960K2U)  
    Butylated Hydroxytoluene (UNII: 1P9D0Z171K)  
    FD&C Red No. 40 (UNII: WZB9127XOA)  
    FD&C Yellow No. 6 (UNII: H77VEI93A8)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    Glycerin (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Water (UNII: 059QF0KO0R)  
    Sorbitan (UNII: 6O92ICV9RU)  
    Sorbitol (UNII: 506T60A25R)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorORANGEScoreno score
    ShapeOVALSize20mm
    FlavorImprint Code AS016
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 66715-6951-06 in 1 CARTON01/28/2019
    12 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34109/05/2014
    COLD AND FLU DAYTIME 
    acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66715-6852
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen325 mg
    Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan Hydrobromide10 mg
    Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV) Phenylephrine Hydrochloride5 mg
    Inactive Ingredients
    Ingredient NameStrength
    Butylated Hydroxyanisole (UNII: REK4960K2U)  
    Butylated Hydroxytoluene (UNII: 1P9D0Z171K)  
    FD&C red No. 40 (UNII: WZB9127XOA)  
    FD&C yellow No. 6 (UNII: H77VEI93A8)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    Glycerin (UNII: PDC6A3C0OX)  
    Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
    Povidone, Unspecified (UNII: FZ989GH94E)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Sorbitan (UNII: 6O92ICV9RU)  
    Sorbitol (UNII: 506T60A25R)  
    Water (UNII: 059QF0KO0R)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorORANGEScoreno score
    ShapeOVALSize20mm
    FlavorImprint Code 512
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 66715-6852-06 in 1 CARTON10/01/201501/28/2022
    12 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34109/05/201401/28/2022
    COLD AND FLU DAYTIME 
    acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66715-6853
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen325 mg
    Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan Hydrobromide10 mg
    Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV) Phenylephrine Hydrochloride5 mg
    Inactive Ingredients
    Ingredient NameStrength
    Butylated Hydroxyanisole (UNII: REK4960K2U)  
    Butylated Hydroxytoluene (UNII: 1P9D0Z171K)  
    FD&C red No. 40 (UNII: WZB9127XOA)  
    FD&C yellow No. 6 (UNII: H77VEI93A8)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    Glycerin (UNII: PDC6A3C0OX)  
    Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
    Povidone, Unspecified (UNII: FZ989GH94E)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Sorbitan (UNII: 6O92ICV9RU)  
    Sorbitol (UNII: 506T60A25R)  
    Water (UNII: 059QF0KO0R)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorORANGEScoreno score
    ShapeOVALSize20mm
    FlavorImprint Code P119
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 66715-6853-06 in 1 CARTON10/01/201501/28/2022
    12 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34109/05/201401/28/2022
    Labeler - Lil' Drug Store Products, Inc (093103646)

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