LASTACAFT- alcaftadine solution/ drops

LASTACAFT by

Drug Labeling and Warnings

LASTACAFT by is a Otc medication manufactured, distributed, or labeled by Allergan, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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?

1.800.678.1605

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)

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)

INGREDIENTS AND APPEARANCE

LASTACAFT 
alcaftadine solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0023-4291
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
alcaftadine (UNII: 7Z8O94ECSX) (alcaftadine - UNII:7Z8O94ECSX)	alcaftadine	2.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0023-4291-05	1 in 1 CARTON	12/01/2021
1		5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 0023-4291-10	2 in 1 CARTON	12/01/2021
2		5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 0023-4291-01	1 in 1 CARTON	12/01/2021
3		1 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4	NDC: 0023-4291-06	1 in 1 CARTON	12/01/2021
4		5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5	NDC: 0023-4291-07	2 in 1 CARTON	12/01/2021
5		5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA022134	12/01/2021

Labeler - Allergan, Inc. (144796497)