FDA Label for Advanced Relief
View Indications, Usage & Precautions
Advanced Relief Product Label
The following document was submitted to the FDA by the labeler of this product American Sales Company. 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
Dextran 70 0.1%
Polyethylene Glycol 400 1%
Povidone 1%
Tetrahydrozoline HCl 0.5%
Purpose
Lubricant
Lubricant
Lubricant
Redness reliever
Use
- relieves redness of the eye due to minor eye irritations
- as a lubricant to prevent further irritation or to relieve dryness of the eye
Warnings
For external use only
Ask A Doctor Before Using If You Have
Narrow angle glaucoma
When Using This Product
- pupils may become enlarged temporarily
- to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
- if solution changes color or becomes cloudy, do not use
- overuse may cause increased redness of the eye
- remove contact lenses before using
Stop Use And Ask A Doctor If
you experience
- eye pain
- changes in vision
- continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours
If Pregnant Or Breast-Feeding,
ask a health professional before use.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Instill 1 or 2 drops in the affected eye(s) up to four times daily.
Other Information
store at 15° to 30°C (59°F to 86°F)
Inactive Ingredients
benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate, sodium chloride
Package Label
Advanced Relief
* Please review the disclaimer below.