Label: SUPRESS A- dexbromopheniramine maleate, dextromethorphan hbr, phenylephrine hcl syrup

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated September 22, 2025

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active ingredients (in each 1 mL)

    Dexbrompheniramine Maleate, 1 mg

    Dextromethorphan HBr, 10 mg

    Phenylephrine HCl, 5 mg

  • Purposes

    Antihistamine

    Cough suppressant

    Nasal decongestant

  • Uses

    • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • sneezing • itchy nose or throat • runny nose • itchy, watery eyes
    • nasal congestion
    • temporarily controls cough due to minor throat and bronchial irritation associated with inhaled irritants
    • temporarily restores freer breathing through nose

  • Warnings

    Do not use 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.

    Ask a doctor before use if the child has
    • heart disease • high blood pressure • thyroid disease • diabetes • glaucoma • cough that occurs with too much phlegm (mucus) • a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis, or emphysema

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

    When using this product
    do not exceed recommended dosage 
    • excitability may occur, especially in children • may cause marked drowsiness • sedatives and tranquilizers may increase drowsiness effect

    Stop use and ask a doctor if • nervousness, dizziness, or sleeplessness occur • new symptoms occur • symptoms do not improve within 7 days or are accompanied by fever • cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache.
    These could be signs of a serious condition.

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

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

  • Directions

    • do not use more than 6 doses in any 24-hour period.
    • repeat every 4 hours.
    • measure with the dosage device provided. Do not use with any other device
    • children 6 to under 12 years of age: 1 mL • children under 6 years of age, consult a docotor.

  • Other information

    • Tamper Evident Feature: Do not use if cap seal is torn, broken or missing.
    • Store at controlled room temperature 15°-30°C (59° to 86°F).
    • Avoid excessive heat and humidity.
  • Inactive ingredients

    Citric acid, flavor, glycerin, methylparaben, polysorbate, propylene glycol, propylparaben, purified water, sodium citrate, sucralose.

  • Questions or comments?

    call weekdays from 8 am to 4 pm AST at 1.787.767.2072

  • SPL UNCLASSIFIED SECTION

    For relief of:
    + Itchy nose or throat
    + Coughs
    + Stuffy nose
    + Sinus congestion

    Sugar, Dye & Alcohol Free

    PSEUDOEPHEDRINE & PPA FREE

    RETAIN CARTON FOR FULL PRESCRIBING INFORMATION

    ​Manufactured in the USA for Kramer Novis, San Juan, PR 00917. www.kramernovis.com

  • Packaging

    Supresss A

  • INGREDIENTS AND APPEARANCE
    SUPRESS A 
    dexbromopheniramine maleate, dextromethorphan hbr, phenylephrine hcl syrup
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52083-057
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP) DEXBROMPHENIRAMINE MALEATE1 mg  in 1 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 1 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorGRAPE (GRAPE) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52083-057-0130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/01/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01208/01/2012
    Labeler - Kramer Novis (090158395)
    Registrant - KRAMER NOVIS (090158395)