Label: TRIPROLIDINE HCL DROPS- triprolidine hydrochloride liquid

  • NDC Code(s): 71321-701-50
  • Packager: Brandywine Pharmaceuticals, LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 8, 2024

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  • SPL UNCLASSIFIED SECTION

    Triprolidine HCl Drops

    NDC 71321-701-50

  • Active ingredients (in each 2 mL)

    Triprolidine HCI 1.25 mg

  • Purpose

    Antihistamine

  • Uses

    ■ temporarily relieves these symptoms due to hay fever

    (allergic rhinitis) or other upper respiratory allergies:

    ■ runny nose ■ itching of the nose or throat

    ■ sneezing ■ itchy, watery eyes

  • Warnings

    Do not exceed recommended dosage.

    Ask a doctor before use if the child has

    ■ a breathing problem such as emphysema or chronic bronchitis

    ■ glaucoma

    ■ trouble urinating due to an enlarged prostate

    Ask a doctor before use if the child is

    taking sedatives or tranquilizers

    When using this product

    ■ excitability may occur, especially in children

    ■ marked drowsiness may occur

    ■ sedatives and tranquilizers may increase the drowsiness effect

    Stop use and ask a doctor if

    ■ new symptoms occur

    Keep out of reach of children.

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

  • Directions

    ■ use only with enclosed dropper   ■ mL= milliliter

    ■ do not use dropper for any other drug product

    children 6 to under 12 years: 2 mL every 6 hours, not to exceed 4 doses in 24 hours, or as directed by a doctor.

    children under 6: ask a doctor.

  • Other information

    ■ read all product information before using

    ■ this packaging is child-resistant.

    ■ store at room temperature 20-30°C (68-86°F)

  • Inactive ingredients

    citric acid anhydrous, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sodium saccharin, sorbitol solution

  • Questions or comments?

    Call 610-314-7943 9 a.m. - 5 p.m. EST.

  • PRINCIPAL DISPLAY PANEL

    NDC 71321-701-50



    Triprolidine HCl Drops



    1.69 fl oz (50 mL)

    LabelCartonPeel_Back

  • INGREDIENTS AND APPEARANCE
    TRIPROLIDINE HCL DROPS 
    triprolidine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71321-701
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890) (TRIPROLIDINE - UNII:2L8T9S52QM) TRIPROLIDINE HYDROCHLORIDE1.25 mg  in 2 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SORBITOL (UNII: 506T60A25R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71321-701-5050 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product03/08/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01203/08/2023
    Labeler - Brandywine Pharmaceuticals, LLC (080581956)
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