Olopatadine Hydrochloride Solution
FDA Label NDC 72476-851

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Retail Business Services, Llc. for the product Olopatadine Hydrochloride (NDC 72476-851). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, purpose, use, warnings, do not use, when using this product, stop use and ask a doctor if you experience:, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active ingredient
Olopatadine (0.2%)
(equivalent to olopatadine hydrochloride, USP 0.222%)

Purpose

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 (1-800-222-1222) right away.

Directions

  • 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

Other Information

  • only for use in the eye
  • store between 2° to 25°C (36° to 77°F)

Inactive Ingredients

benzalkonium chloride 0.01%, dibasic sodium phosphate, edetate disodium, hydrochloric acid/sodium hydroxide (adjust pH), povidone, sodium chloride and water for injection

Questions?

✆ 1-866-850-2876

DISTRIBUTED BY:
FOODHOLD U.S.A., LLC,
LANDOVER, MD 20785
MADE IN INDIA

Package Label-Principal Display Panel-0.2% (2.5 Ml Container)

CAREone        NDC 72476-851-21
EYE ALLERGY ITCH RELIEF
Olopatadine Hydrochloride
Ophthalmic Solution USP, 0.2%
Antihistamine
STERILE           2.5 mL (0.085 FL OZ)


Olopatadine-figure-1 (Olopatadine Fig1)

Olopatadine-figure-1 (Olopatadine Fig1)

Package Label-Principal Display Panel-0.2% (2.5 Ml Container Carton)

                                         NDC 72476-851-21
CAREone
Compare to the Active Ingredient in
Pataday® Once Daily Relief

EYE ALLERGY
ITCH RELIEF
Olopatadine Hydrochloride
Ophthalmic Solution USP, 0.2%

ONCE DAILY
Now available without a prescription
Antihistamine
Works in Minutes
Relief from Allergens:
Pet Dander, Pollen, Grass, Ragweed

STERILE
2.5 mL (0.085 FL OZ)


Olopatadine-figure-2 (Olopatadine Fig2)

Olopatadine-figure-2 (Olopatadine Fig2)

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