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Pataday Twice Daily Relief Prescribing Information

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

Medically reviewed by Drugs.com. Last updated on Aug 24, 2023.

Active IngredientsPurpose
Olopatadine (0.1%).
(equivalent to olopatadine hydrochloride 0.111%)
Antihistamine and Redness Reliever

Use temporarily relieves itchy and red 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.

Pataday Twice Daily Relief Dosage and Administration

  • adults and children 2 years of age and older:
    • put 1 drop in the affected eye(s) twice daily, every 6 to 8 hours, no more than twice 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

Storage and Handling

  • only for use in the eye
  • store between 4°-25°C (39°-77°F)

Inactive ingredients

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

Questions?

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

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

NDC: 0065-4274-01
9017919-1219

PRINCIPAL DISPLAY PANEL

NOW AVAILABLE
without a prescription

Pataday®
TWICE DAILY RELIEF
Olopatadine hydrochloride
ophthalmic solution 0.1%
Antihistamine and Redness Reliever

Eye Allergy Itch & Redness Relief
TWICE DAILY

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

STERILE
5 mL (0.17 FL OZ)

Alcon

Pataday®

TWICE DAILY RELIEF
Eye Allergy Itch & Redness Relief
Works in Minutes

For Ages 2 and Older
30 DAY SUPPLY

TAMPER EVIDENT: For your protection, this bottle has a seal imprinted with Alcon around the neck.

________Fill Line________

Do not use if seal is damaged or missing at time of purchase.

ACTUAL SIZE

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


NDC: 0065-4274-01
9017919-1219

LOT: EXP.:

carton
carton

Pataday®
TWICE DAILY RELIEF
Olopatadine hydrochloride
ophthalmic solution 0.1%
Antihistamine and Redness Reliever
Eye Allergy Itch & Redness Relief

5 mL (0.17 FL OZ)
STERILE

Only for use in the eye.
Store between 4° – 25° C (39° – 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.
6201 South Freeway
Fort Worth, TX 76134

LOT: EXP.:

H15723-1219

label
PATADAY TWICE A DAY RELIEF
olopatadine hydrochloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0065-4274
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Olopatadine Hydrochloride (UNII: 2XG66W44KF) (Olopatadine - UNII:D27V6190PM) Olopatadine1 mg in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Phosphate, Dibasic, Unspecified Form (UNII: GR686LBA74)
Sodium Chloride (UNII: 451W47IQ8X)
Benzalkonium Chloride (UNII: F5UM2KM3W7)
Hydrochloric Acid (UNII: QTT17582CB)
Sodium Hydroxide (UNII: 55X04QC32I)
Water (UNII: 059QF0KO0R)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0065-4274-011 in 1 CARTON02/28/2020
15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02068802/28/2020
Labeler - Alcon Laboratories, Inc. (008018525)
Establishment
NameAddressID/FEIBusiness Operations
Alcon Research LLC007672236manufacture(0065-4274)