FDA Label for Rohto Optic Glow
View Indications, Usage & Precautions
Rohto Optic Glow Product Label
The following document was submitted to the FDA by the labeler of this product The Mentholatum 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 Ingredients
Naphazoline hydrochloride 0.03%
Povidone 0.5%
Propylene glycol 0.2%
Purpose
Naphazoline hydrochloride - Redness reliever
Povidone – Lubricant
Propylene glycol - Lubricant
Uses
• relieves redness of the eye due to minor eye irritations• temporarily relieves burning and irritation due to dryness of the eye
Warnings
For external use only
Ask A Doctor Before Use If You Have
narrow angle glaucoma
When Using This Product
• do not touch tip of container to any surface to avoid contamination• replace cap after each use• do not use if solution changes color or becomes cloudy• overuse of this product may produce increased redness of the eye• pupils may become enlarged temporarily
Stop Use And Ask A Doctor If
• you experience eye pain• changes in vision occur• redness or irritation of the eyes lasts• condition worsens or lasts more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• put 1 or 2 drops in the affected eye(s) up to 4 times daily• tightly snap on cap to seal
Other Safety Information
• do not store above 25°C (77°F)
Inactive Ingredients
anhydrous citric acid, boric acid, chlorobutanol, edetate disodium, menthol, polysorbate 80, potassium aspartate, purified water, pyridoxine hydrochloride, sodium borate, sodium citrate, sodium hyaluronate
Questions?
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