Active Ingredients
Glycerin (0.6%)
Propylene Glycol (0.6%)
Soothe Solution/ Drops
FDA Label NDC 24208-495
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bausch & Lomb Incorporated for the product Soothe (NDC 24208-495). 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 active ingredients, purpose, uses, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Lubricant
Lubricant
Uses
- relieves dryness of the eye
- prevents further irritation
Do Not Use
- if solution changes color or becomes cloudy
- if single-unit dispenser is not intact
When Using This Product
- do not touch tip of container to any surface to avoid contamination
- once opened, discard
- do not reuse
Stop Use And Ask A Doctor If
- you experience eye pain, changes in vision, continued redness or irritation of the eye
- condition worsens or persists for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- to open, completely twist off tab
- instill 1 to 2 drops in the affected eye(s) as needed
Other Information
- store at 15°- 25°C (59°- 77°F)
Inactive Ingredients
boric acid, hydroxyalkylphosphonate, purified water, sodium alginate, sodium borate
Questions?
Call: 1-800-553-5340
Package/Label Principal Display Panel
Bausch & Lomb
Soothe®
Lubricant Eye Drops
PRESERVATIVE FREE
Dry Eye Therapy
0.02 FL OZ EA (0.6 mL EA) 28 Sterile Single-Use Dispensers
* Please review the disclaimer below.
