Label: PATADAY ONCE DAILY RELIEF- olopatadine hydrochloride solution
- NDC Code(s): 0065-8150-01, 0065-8150-03, 0065-8150-04, 0065-8150-07
- Packager: Alcon Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 21, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- Do not use
- When using this product
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Questions?
-
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.:
H15725-219Original 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
-
INGREDIENTS AND APPEARANCE
PATADAY ONCE DAILY RELIEF
olopatadine hydrochloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0065-8150 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Olopatadine Hydrochloride (UNII: 2XG66W44KF) (Olopatadine - UNII:D27V6190PM) Olopatadine 2 mg in 1 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:0065-8150-01 1 in 1 CARTON 02/28/2020 1 2.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:0065-8150-03 2 in 1 CARTON 02/28/2020 2 2.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:0065-8150-04 1 in 1 CARTON 02/28/2020 3 0.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:0065-8150-07 3 in 1 CARTON 01/15/2021 4 2.5 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 NDA021545 02/28/2020 Labeler - Alcon Laboratories, Inc. (008018525) Establishment Name Address ID/FEI Business Operations Alcon Research LLC 007672236 manufacture(0065-8150)