Label: SPRINSOL- chlorpheniramine maleate tablet

  • NDC Code(s): 51467-101-01, 51467-101-02
  • Packager: FORTUNE PHARMACAL COMPANY LIMITED
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 13, 2025

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active ingredients (in each tablet)
    Chlorpheniramine maleate 4 mg

  • PURPOSE

    Purpose
    Antihistamine

  • INDICATIONS & USAGE

    Uses
    temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies:
    sneezing
    runny nose
    itching of the nose or throat
    itchy, watery eyes

  • WARNINGS

    Warnings
    Ask a doctor before use if you have
    a breathing problem such as emphysema or chronic bronchitis
    glaucoma
    difficulty in urination due to enlargement of the prostate gland

  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if you are
    taking sedatives or tranquilizers

  • WHEN USING

    When using this product
    do not exceed recommended dosage unless directed by a physician
    may cause excitability especially in children
    use caution when driving or operating machinery
    avoid alcoholic beverages
    may cause drowsiness; alcohol, sedatives, and tranquilizers may increase the drowsiness effect

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away

  • DOSAGE & ADMINISTRATION

    Directions
    adults and children 12 years of age and over: take 1 tablet every 4 to 6 hours, not to exceed 6 tablets (24 mg) in 24 hours, or as directed by a doctor
    children under 12 years of age: consult a doctor

  • OTHER SAFETY INFORMATION

    Other information
    keep tightly sealed
    protect from light
    store between 20 to 25 C (68 to 77 F)

  • INACTIVE INGREDIENT

    Inactive ingredients
    colloidal silicon dioxide, corn starch, FD C red no. 40 aluminum lake, lactose monohydrate, magnesium stearate, povidone K30, sodium starch glycolate

  • QUESTIONS

    Questions or comments? (888) 221-3496 M-F 9 am to 5 pm
    you may also report serious side effects to this phone number

  • PRINCIPAL DISPLAY PANEL

    Sprinsol

    Safely Sealed

    NDC 51467-101-02

    Chlorpheniramine maleate - Antihistamine

    temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies:
    sneezing
    runny nose
    itching of the nose or throat
    itchy, watery eyes

    36 Tablets

    In Individually Sealed Strip

    Respiratory Series
    IMAGE OF CARTON

  • INGREDIENTS AND APPEARANCE
    SPRINSOL 
    chlorpheniramine maleate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51467-101
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE4 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POVIDONE K30 (UNII: U725QWY32X)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    Product Characteristics
    ColorredScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code FORTUNE
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51467-101-012 in 1 BOX09/22/2017
    112 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:51467-101-023 in 1 BOX09/22/2017
    212 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01209/22/2017
    Labeler - FORTUNE PHARMACAL COMPANY LIMITED (686280561)
    Registrant - FORTUNE PHARMACAL COMPANY LIMITED (686280561)
    Establishment
    NameAddressID/FEIBusiness Operations
    FORTUNE PHARMACAL COMPANY LIMITED686280561manufacture(51467-101)