Label: OPCON-A- naphazoline hydrochloride and pheniramine maleate solution/ drops

  • NDC Code(s): 24208-430-03, 24208-430-15, 24208-430-30, 24208-430-45
  • Packager: Bausch & Lomb Incorporated
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated December 14, 2023

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  • Active ingredients

    Naphazoline HCl (0.02675%)

    Pheniramine maleate (0.315%)

  • Purposes

    Redness reliever

    Antihistamine

  • Uses

    •
    temporarily relieves itching and redness caused by pollen, ragweed, grass, animal hair and dander
  • Warnings

    For external use only

    Do not use

    •
    if you are sensitive to any ingredient in this product
    •
    if solution changes color or becomes cloudy

    Ask a doctor before use if you have

    •
    heart disease
    •
    high blood pressure
    •
    trouble urinating due to an enlarged prostate gland
    •
    narrow angle glaucoma

    When using this product

    •
    overuse may cause more eye redness
    •
    pupils may become enlarged temporarily
    •
    do not touch tip of container to any surface to avoid contamination
    •
    you may feel a brief tingling after putting drops in eye
    •
    replace cap after use
    •
    remove contact lenses before using

    Stop use and ask a doctor if you experience

    •
    eye pain
    •
    changes in vision
    •
    redness or irritation of the eye that worsens or lasts more than 72 hours

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away. Accidental oral ingestion in infants and children may lead to coma and marked reduction in body temperature.

  • Directions

    •
    Adults and children 6 years of age and older: Instill 1 or 2 drops in the affected eye(s) up to 4 times daily.
    •
    Children under 6 years: ask a doctor
  • Other information

    •
    store at 20-25 °C (68-77 °F)
    •
    this package is child-resistant
    •
    protect from light
    •
    use before expiration date marked on the carton or bottle
  • Inactive ingredients

    benzalkonium chloride, boric acid, edetate disodium, hypromellose, purified water, sodium borate, sodium chloride. Hydrochloric acid may be used to adjust pH.

  • Questions or comments?

    [phone icon] call: 1-800-553-5340

    Distributed by:
    Bausch & Lomb Americas Inc.
    Bridgewater, NJ 08807 USA

  • Package/Label Principal Display Panel

    CARTON

    TWIN PACK

    NDC 24208-430-45

    BAUSCH + LOMB

    Opcon-A®
    pheniramine maleate 0.315% and naphazoline
    hydrochloride 0.02675% ophthalmic solution
    ANTIHISTAMINE AND REDNESS RELIEVER

    EYE DROPS
    CLINICALLY PROVEN
    EYE ALLERGY RELIEF

    itching + redness

    caused by pollen, ragweed, grass, animal hair and dander

    [teardrop icon]

    STERILE
    2 x 15 mL BOTTLES
    (0.5 FL OZ EACH)

    3844801
    AB55299

  • INGREDIENTS AND APPEARANCE
    OPCON-A 
    naphazoline hydrochloride and pheniramine maleate solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-430
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.2675 mg  in 1 mL
    PHENIRAMINE MALEATE (UNII: NYW905655B) (PHENIRAMINE - UNII:134FM9ZZ6M) PHENIRAMINE MALEATE3.15 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BORIC ACID (UNII: R57ZHV85D4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24208-430-031 in 1 CARTON08/06/199404/01/2013
    13 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:24208-430-151 in 1 CARTON08/06/1994
    215 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    3NDC:24208-430-301 in 1 CARTON08/06/199407/01/2011
    330 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    4NDC:24208-430-452 in 1 CARTON07/01/2015
    415 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02006506/08/1994
    Labeler - Bausch & Lomb Incorporated (196603781)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bausch & Lomb Incorporated079587625MANUFACTURE(24208-430)
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