PATADAY ONCE DAILY RELIEF- olopatadine hydrochloride solution 
Alcon Laboratories, Inc.

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Drug Facts

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

When using this product

Stop use and ask a doctor if you experience:

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

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

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:

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)

Revised: 12/2023
Document Id: 30e4fc2d-7d06-477a-9160-aa231b83e642
Set id: 1c7d2342-ba1c-4244-9814-d92a05725d4e
Version: 6
Effective Time: 20231215
 
Alcon Laboratories, Inc.