FDA Label for Hypromellose Eye Drops 0.7%
View Indications, Usage & Precautions
Hypromellose Eye Drops 0.7% Product Label
The following document was submitted to the FDA by the labeler of this product Aurolab. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Hypromellose 0.7% BP w/v
Directions For Use
- lnstill 1or 2 drops in the affected eye, as needed
Inactive Ingredient
- Benzalkonium Chloride
- Borax
- Boric acid
- EDTA disodium salt
- Potassium chloride
- Purified water
- Sodiumchloride
Tamper Protection
- For your protection a tamper evident ring is attached to the bottlecap
- Upon opening, this will separate from the cap and can be discarded
- Use only if this ring is present and attached when the bottle is first opened
Use
- For use as a lubricant to prevent further irritation or to relieve dryness of the eye
Questions
Call: 1-800-103-7321
Email: [email protected]
Web: www.aurolab.com
Keep Out Of Reach Of Children
- If swallowed, get medical help or contact a poison control center right away
Ask Doctor
- If you experience eye pain
- Change in vision
- Continued redness(or) irritation of the eye
- Condition worsens or persists for more than 72 hours
Do Not Use
- If you are sensitive to any ingredient in this product
- If solution changes color or becomes cloudy
Dosage
Instill 1 or 2 drops in the affected eyes as needed
Warnings
For External Use Only
Indications And Usage
For use as a lubricant to prevent further irritaion or to relieve dryness of the eye
Eye Lubricant
Eye Lubricant
Carton Label
Hypromellose.jpg
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