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Day Time Cold Multi-Symptom Cool Blast (Aaron Industries, Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 237 mL in 1 BOTTLE, PLASTIC (49580-0192-8) Label Information

Complete Day Time Cold Multi-Symptom Cool Blast Information

  • Active Ingredients

    Acetaminophen 325 mg
    Guaifenesin 200 mg
    Dextromethorphan HBr 10 mg
    Phenylephrine HCI 5 mg


  • Purposes

    Acetaminophen...........................Pain reliever/fever reducer
    Guaifenesin..........Chest Congestion
    Dextromethorphan HBr..............Cough suppressant
    Phenylephrine HCI......................Nasal decongestant


  • Uses

    temporarily relieves the following cold/flu
    symptoms: minor aches and pains cough
    headache  temporarily reduces fever congestion stuffy nose


  • Warnings

    Liver warning: This product contains acetaminophen.
    Severe liver damage may occur if your child takes:
    more than 5 doses in 24 hours, which is the
    maximum daily amount
    with other drugs containing acetaminophen


  • Do Not Use

    to make a child sleepy
    in a child who is taking a prescription monoamine
    oxidase inhibitor (MAOI) (certain drugs for
    depression, psychiatric or emotional conditions, or
    Parkinson’s disease), or for 2 weeks after stopping
    the MAOI drug. If you do not know if your child's
    prescription drug contains an MAOI, ask a doctor
    or pharmacist before giving this product.
    with any other drug containing acetaminophen
    (prescription or non-prescription). If you are not
    sure whether a drug contains acetaminophen,
    ask a doctor or pharmacist.


  • Ask a doctor before use if the child has

    a breathing problem such as chronic bronchitis
    persistent or chronic cough such as occurs with
    asthma cough that occurs with too much phlegm
    (mucus) heart disease high blood pressure
    thyroid disease diabetes glaucoma liver disease


  • Ask a doctor or pharmacist before use if the child is taking

    sedatives or tranquilizers
    the blood thinning drug warfarin


  • When using this product

    do not exceed recommended dosage (see overdose warning)
    may cause excitability, especially in children
    marked drowsiness may occur sedatives and
    tranquilizers may increase drowsiness


  • Stop use and ask a doctor if

    new symptoms occur
    fever gets worse or lasts for more than 3 days
    redness or swelling is present
    pain, nasal congestion or cough gets worse or
    lasts for more than 5 days
    nervousness, dizziness or sleeplessness occur
    cough comes back or occurs with rash or headache
    that lasts. These could be signs of a serious
    condition


  • Keep this and all drugs out of the reach of children.

    Overdose Warning: Taking more than the
    recommended dose (overdose) could cause serious
    health problems, including liver damage. In case of
    accidental overdose, seek professional assistance or
    contact a Poison Control Center immediately. Quick
    medical attention is critical even if you do not notice
    any signs or symptoms.


  • Directions

    do not exceed recommended dosage
    (see overdose warning) Use the dosage cup provided

    Age (yr)                                                                                            Dose (tsp or mL)
    children under the age of 12; this will provide more                              do not usethis product on children under 12 years of age

    than the recommended dose (overdose) and may

    cause liver damage                                 

    Adults and children 12 years of age and older:                                     Take 2 tbsp (30mL) in dosage cup provided every 4 hours

                                                                                                            Do not take more than 12 tbsp (180mL) in 24 hours


  • Other Information

    store at controlled room temperature


  • Inactive Ingredients

    blue 1, citric acid, flavors, glycerin, purified water, 
    sodium benzoate, sorbitol, sucralose, sorbitol, propylene glycol


  • Principal Display Panel

    Cold Multi-Symptom Cool Blast

    Daytime

    Acetaminophen Fever and sore throat

    Dextromethorphan HBr Cough

    Guaifenesin Chest congestion

    Phenylephrine HCI stuffy nose

    For ages 12 and over

    alcohol .5 percent

    Compare to active ingredient in Tylenol Cold multi-symptom daytime

    Manufactured by Aaron Industries, Inc PO box 801 Lynwood CA 90262

    8 fl oz 237mL

    image of label

  • INGREDIENTS AND APPEARANCE
    DAY TIME COLD MULTI-SYMPTOM COOL BLAST 
    tylenol multi symptom cool blast daytime liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:49580-0192
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg  in 5 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg  in 5 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg  in 5 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor MINT (Mint Flavor) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49580-0192-8 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/2010
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part341 01/01/2010
    Labeler - P & L Development, LLC (101896231)