Label: LASTACAFT- alcaftadine solution/ drops

  • NDC Code(s): 0023-4291-01, 0023-4291-05, 0023-4291-06, 0023-4291-07, view more
    0023-4291-10
  • Packager: Allergan, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated August 10, 2022

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

View All Sections
  • Active ingredient

    Alcaftadine 0.25%

  • Purpose

    Antihistamine

  • Use

    temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander

  • Warnings

    For external use only

    Do not use

    ■ if solution changes color or becomes cloudy

    ■ if you are sensitive to any ingredient in this product

    ■ to treat contact lens related irritation

    When using this product

    ■ do not touch tip of container to any surface to avoid contamination

    ■ remove contact lenses before use

    ■ wait at least 10 minutes before reinserting contact lenses after use

    ■ do not wear a contact lens if your eye is red

    Stop use and ask a doctor if

    you experience any of the following:

    ■ eye pain

    ■ changes in vision

    ■ increased redness of the eye

    ■ itching that worsens or lasts for more than 72 hours

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • adults and children 2 years of age and older: 
      • put 1 drop in the affected eye(s) once daily
      • if using other ophthalmic products while using this product, wait at least 5 minutes between each product
      • replace cap after each use

    • children under 2 years of age: consult a doctor
  • Other information   

    ■ only for use in the eye

    ■ store at 15°-25°C (59°-77°F)

  • Inactive ingredients

    benzalkonium chloride 0.005%, edetate disodium, monobasic sodium phosphate, purified water, sodium chloride, sodium hydroxide and/or hydrochloric acid

  • Questions or comments?

    telephone icon1.800.678.1605

  • PRINCIPAL DISPLAY PANEL

    NDC 0023-4291-10
    ORIGINAL
    PRESCRIPTION STRENGTH
    LASTACAFT    ®
    Alcaftadine ophthalmic solution 0.25%
    Antihistamine Eye Drops
    ONCE DAILY RELIEF
    Eye Allergy Itch Relief
    WORKS IN MINUTES
    RELIEF FROM ALLERGENS:
    Pet Dander Pollen Grass Ragweed
    STERILE
    120 DAY SUPPLY
    Two 5 mL bottles (0.17 fl oz each)

    NDC 0023-4291-10 ORIGINAL PRESCRIPTION STRENGTH LASTACAFT® Alcaftadine ophthalmic solution 0.25% Antihistamine Eye Drops ONCE DAILY RELIEF Eye Allergy Itch Relief WORKS IN MINUTES RELIEF FROM ALLERGENS: Pet Dander Pollen Grass Ragweed STERILE 120 DAY SUPPLY Two 5 mL bottles (0.17 fl oz each)

  • PRINCIPAL DISPLAY PANEL

    NDC 0023-4291-05
    ORIGINAL
    PRESCRIPTION STRENGTH
    LASTACAFT    ®
    Alcaftadine ophthalmic solution 0.25%
    Antihistamine Eye Drops
    ONCE DAILY RELIEF
    Eye Allergy Itch Relief
    WORKS IN MINUTES
    RELIEF FROM ALLERGENS:
    Pet Dander Pollen Grass Ragweed
    STERILE
    60 DAY SUPPLY
    0.17 fl oz (5 mL)

    NDC 0023-4291-05 ORIGINAL PRESCRIPTION STRENGTH LASTACAFT® Alcaftadine ophthalmic solution 0.25% Antihistamine Eye Drops ONCE DAILY RELIEF Eye Allergy Itch Relief WORKS IN MINUTES RELIEF FROM ALLERGENS: Pet Dander Pollen Grass Ragweed STERILE 60 DAY SUPPLY 0.17 fl oz (5 mL)

  • INGREDIENTS AND APPEARANCE
    LASTACAFT 
    alcaftadine solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-4291
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    alcaftadine (UNII: 7Z8O94ECSX) (alcaftadine - UNII:7Z8O94ECSX) alcaftadine2.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    benzalkonium chloride (UNII: F5UM2KM3W7)  
    edetate disodium (UNII: 7FLD91C86K)  
    sodium phosphate, monobasic (UNII: 3980JIH2SW)  
    water (UNII: 059QF0KO0R)  
    sodium chloride (UNII: 451W47IQ8X)  
    sodium hydroxide (UNII: 55X04QC32I)  
    hydrochloric acid (UNII: QTT17582CB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0023-4291-051 in 1 CARTON12/01/2021
    15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:0023-4291-102 in 1 CARTON12/01/2021
    25 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3NDC:0023-4291-011 in 1 CARTON12/01/2021
    31 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4NDC:0023-4291-061 in 1 CARTON12/01/2021
    45 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    5NDC:0023-4291-072 in 1 CARTON12/01/2021
    55 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02213412/01/2021
    Labeler - Allergan, Inc. (144796497)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!