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Pataday Once Daily Relief

Package insert / prescribing information
Generic name: olopatadine hydrochloride
Dosage form: ophthalmic solution
Drug class: Ophthalmic antihistamines and decongestants

Medically reviewed by Drugs.com. Last updated on Dec 1, 2021.

Active Ingredients Purpose
Olopatadine 0.2%
(equivalent to olopatadine hydrochloride 0.222%)
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:

  • eye pain
  • changes in vision
  • increased redness of the eye
  • itching 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, no more than once per day
    • 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 between 2°-25°C (36°-77°F)

Inactive ingredients

benzalkonium chloride 0.01%, dibasic sodium phosphate, edetate disodium, hydrochloric acid/sodium hydroxide (adjust pH), povidone, purified water, and sodium chloride

Questions?

In the U.S., call 1-800-757-9195 or email alcon.medinfo@alcon.com

PRINCIPAL DISPLAY PANEL

NOW AVAILABLE
without a prescription

Pataday®
ONCE DAILY RELIEF
Olopatadine hydrochloride
ophthalmic solution 0.2%
Antihistamine

Eye Allergy Itch Relief

ONCE DAILY

Works in Minutes
Relief from Allergens:
• Pet Dander
• Pollen
• Grass
• Ragweed

STERILE
2.5 mL (0.085 FL OZ)

Alcon

Pataday®

ONCE DAILY RELIEF

Eye Allergy Itch Relief
Works in Minutes

TAMPER EVIDENT: For your protection, this bottle has a seal imprinted with Alcon around the neck. Do not use if seal is damaged or missing at time of purchase.

For Ages 2 and Older
30 DAY SUPPLY

________Fill Line________

6201 South Freeway
Fort Worth, Texas 76134
Country of Origin: Japan

ACTUAL SIZE

NDC: 0065-8150-01
9017921-1219

Pataday®
ONCE DAILY RELIEF
Olopatadine hydrochloride
ophthalmic solution 0.2% Antihistamine

2.5 mL (0.085 FL OZ)
STERILE

EYE ALLERGY ITCH RELIEF
Only for use in the eye. Store between 2°– 25° C (36°– 77° F)

TAMPER EVIDENT: For your protection, this bottle has a seal imprinted with Alcon around the neck. Do not use if seal is damaged or missing at time of purchase.

Alcon Laboratories, Inc.
Fort Worth, TX 76134

LOT: EXP.:

H15725-219

Original Prescription Strength

Pataday

ONCE DAILY RELIEF

Olopatadine hydrochloride
ophthalmic solution 0.2%
Antihistamine

Eye Allergy Itch Relief

ONCE DAILY

Works in Minutes Relief from Allergens:

  • Pet Dander
  • Pollen
  • Grass
  • Ragweed

STERILE

2.5 mL (0.085 FL OZ)

Alcon

Pataday

ONCE DAILY RELIEF

Eye Allergy Itch Relief
Works in Minutes

TAMPER EVIDENT: For your protection,
this bottle has a seal imprinted with Alcon
around the neck. Do not use if seal is
damaged or missing at time of purchase.


For Ages 2
and Older
30 DAY
SUPPLY
________Fill Line________

Alcon Laboratories, Inc.
6201 South Freeway
Fort Worth, Texas 76134
Country of Origin: Japan

ACTUAL SIZE

NDC: 0065-6150-01 300037159-0520

Pataday Once Daily Relief
olopatadine hydrochloride solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0065-8150
Route of Administration OPHTHALMIC DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Olopatadine Hydrochloride (Olopatadine) Olopatadine 2 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
Povidone, Unspecified
Sodium Phosphate, Dibasic, Unspecified Form
Sodium Chloride
Edetate Disodium
Benzalkonium Chloride
Hydrochloric Acid
Sodium Hydroxide
Water
Packaging
# Item Code Package Description
1 NDC:0065-8150-01 1 BOTTLE, PLASTIC in 1 CARTON
1 2.5 mL in 1 BOTTLE, PLASTIC
2 NDC:0065-8150-03 2 BOTTLE, PLASTIC in 1 CARTON
2 2.5 mL in 1 BOTTLE, PLASTIC
3 NDC:0065-8150-04 1 BOTTLE, PLASTIC in 1 CARTON
3 0.5 mL in 1 BOTTLE, PLASTIC
4 NDC:0065-8150-07 3 BOTTLE, PLASTIC in 1 CARTON
4 2.5 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021545 02/28/2020
Labeler - Alcon Laboratories, Inc. (008018525)
Establishment
Name Address ID/FEI Operations
Alcon Research LLC 007672236 manufacture(0065-8150)
Alcon Laboratories, Inc.