PANCOLD S (GUAIFENESIN) LIQUID [KAFUS CO., LTD]

PANCOLD S (GUAIFENESIN) LIQUID [KAFUS CO., LTD]
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NDC 55277-1001-1
Set ID 52726d93-b3ba-432f-96f6-d03bf9f7b840
Category HUMAN OTC DRUG LABEL
Packager Kafus Co., Ltd
Generic Name
Product Class
Product Number
Application Number PART341
  • ACTIVE INGREDIENT

    Guaifenesin
    Caffeine anhydrous
    Chlorpheniramine maleate
    dl-methylephedrine hydrochloride
    Acetaminophen
  • INACTIVE INGREDIENT

    alcohol, citric acid, edentate sodium, high fructose corn syrup, lemon essence, methylparaben, monosodium glutamate, orange essence, propylene glycol, propylparaben, sodium benzoate, sodium chloride, water, tartrazine
  • PURPOSE

    Temporarily relieves these minor symptoms due to a cold or the flu:
    ▪aches ▪pain ▪headache ▪sore throat ▪muscular aches ▪fever
    ▪rummy nose ▪sneezing ▪itching of the nose and throat
    ▪nasal congestion ▪sinus congestion and pressure
    ▪cough due to minor throat and bronchial irritation
  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children
  • INDICATIONS & USAGE

    Adults and children 12 years and older: Take 1 bottle every 4 hours, while symptoms persist not to exceed 6 bottles in 24 hours, or as directed by a doctor.
  • WARNINGS

    Alcohol warning:
    ▪If you consume 3 or more alcoholic drinks every day, ask your doctor whether you should take acetaminophen or other pain relievers/fever reducers. ▪Acetaminophen may cause liver damage.
  • DOSAGE & ADMINISTRATION

    for oral use only
  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    PANCOLD S  
    guaifenesin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55277-1001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN83.3 mg  in 30 mL
    CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE30 mg  in 30 mL
    CHLORPHENIRAMINE (UNII: 3U6IO1965U) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE2.5 mg  in 30 mL
    METHYLEPHEDRINE HYDROCHLORIDE, DL- (UNII: 99214P83XM) (METHYLEPHEDRINE, DL- - UNII:SHS9PGQ2LS) METHYLEPHEDRINE HYDROCHLORIDE, DL-17.5 mg  in 30 mL
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN300 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    LEMON (UNII: 24RS0A988O)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MONOSODIUM GLUTAMATE (UNII: W81N5U6R6U)  
    ORANGE (UNII: 5EVU04N5QU)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55277-1001-130 mL in 1 BOTTLE, GLASS
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34101/15/2013
    Labeler - Kafus Co., Ltd (688445679)
    Registrant - Kafus Co., Ltd (688445679)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dong Hwa Pharm Co., Ltd687745240manufacture(55277-1001)

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