Label: OPHTHAVET COMPLETE- hyaluronate sodium gel
- NDC Code(s): 17033-046-10
- Packager: Dechra Veterinary Products
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated March 18, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- CONTAINS:
- INDICATIONS:
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CAUTION:
If condition worsens, discontinue use and consult veterinarian. Keep container tightly closed. To avoid contamination, do not touch tip of container to any surface including the eye, the eyelid or your fingers. Replace cap after using. To minimize the risk of infection, DO NOT use beyond the expiry date on the label. Do not use if safety seal is broken. Do not use if cloudy or discolored.
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DIRECTIONS:
Apply to the eye as directed by your veterinarian.
OPHTHAVET Complete Ophthalmic Gel provides blink-activated lubrication and moistening for the eye surface during the day or night.
- Wash hands before use.
- Tilt the animal's head up slightly and pull the lower eyelid down to create a small area to apply the drop.
- While holding the bottle above the eye, press gently to release one drop onto the eye.
- Repeat the process in the other eye, if needed.
- After application, shake any remaining droplet from the tip of bottle and replace cap securely. This will help to prevent contamination of the bottle.
- Can be applied as often as directed by your veterinarian.
- If you are applying any other eye drops or ointments, wait at least 15 minutes between each application.
- STORAGE AND HANDLING
- WARNINGS
- HOW SUPPLIED:
- MANUFACTURED FOR:
- PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
OPHTHAVET COMPLETE
hyaluronate sodium gelProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:17033-046 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 2 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17033-046-10 1 in 1 CARTON 1 10 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 09/01/2021 Labeler - Dechra Veterinary Products (362142734)
