Label: OLOPATADINE HYDROCHLORIDE solution
- NDC Code(s): 79903-000-40
- Packager: Wal-Mart Stores, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated June 21, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if you experience:
- Keep Out of Reach of Children.
-
Directions
-
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
-
adults and children 2 years of age and older:
- Other information
- Inactive ingredients
- Questions?
- PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.1% (5 mL Container)
-
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.1% (5 mL Container Carton)
NDC 79903-000-40
equateTM
Compare to Pataday® Twice Daily Relief active ingredient*
NOW AVAILABLE
WITHOUT A PRESCRIPTION
Olopatadine
Hydrochloride
Ophthalmic Solution
USP, 0.1%
Antihistamine and
Redness Reliever
EYE ALLERGY ITCH & REDNESS RELIEF
Works in Minutes
Relief from Allergens:
• Pet Dander • Pollen
• Grass • Ragweed
TWICE DAILY
STERILE
5 mL (0.17 FL OZ)
-
INGREDIENTS AND APPEARANCE
OLOPATADINE HYDROCHLORIDE
olopatadine hydrochloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-000 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OLOPATADINE HYDROCHLORIDE (UNII: 2XG66W44KF) (OLOPATADINE - UNII:D27V6190PM) OLOPATADINE HYDROCHLORIDE 1 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74) SODIUM CHLORIDE (UNII: 451W47IQ8X) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-000-40 1 in 1 CARTON 07/15/2020 1 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 ANDA ANDA204812 07/15/2020 Labeler - Wal-Mart Stores, Inc. (051957769)