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Pataday Once 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 0.2%
(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.

Pataday Once Daily Relief Dosage and Administration

  • 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

Storage and Handling

  • 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

carton

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

label

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

300037159-0520
PATADAY ONCE DAILY RELIEF
olopatadine hydrochloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0065-8150
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Olopatadine Hydrochloride (UNII: 2XG66W44KF) (Olopatadine - UNII:D27V6190PM) Olopatadine2 mg in 1 mL
Inactive Ingredients
Ingredient NameStrength
Povidone, Unspecified (UNII: FZ989GH94E)
Sodium Phosphate, Dibasic, Unspecified Form (UNII: GR686LBA74)
Sodium Chloride (UNII: 451W47IQ8X)
Edetate Disodium (UNII: 7FLD91C86K)
Benzalkonium Chloride (UNII: F5UM2KM3W7)
Hydrochloric Acid (UNII: QTT17582CB)
Sodium Hydroxide (UNII: 55X04QC32I)
Water (UNII: 059QF0KO0R)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0065-8150-011 in 1 CARTON02/28/2020
12.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:0065-8150-032 in 1 CARTON02/28/2020
22.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:0065-8150-041 in 1 CARTON02/28/2020
30.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:0065-8150-073 in 1 CARTON01/15/2021
42.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02154502/28/2020
Labeler - Alcon Laboratories, Inc. (008018525)
Establishment
NameAddressID/FEIBusiness Operations
Alcon Research LLC007672236manufacture(0065-8150)