SOOTHE- glycerin and propylene glycol solution/ drops 
Bausch & Lomb Incorporated

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Soothe Preservative Free Drug Facts

Active ingredients

Glycerin (0.6%)

Propylene glycol (0.6%)

Purpose

Lubricant

Lubricant

Uses

•
relieves dryness of the eye
•
prevents further irritation

Warnings

For external use only
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
•
discard dispenser immediately after use

Other information

•
store at 15 – 25 °C (59 – 77 °F)

Inactive ingredients

boric acid, hydroxyalkylphosphonate, purified water, sodium alginate, sodium borate

Questions?

[phone icon] Call: 1-800-553-5340

Marketed by:
Bausch & Lomb Americas Inc.
Bridgewater, NJ 08807 USA

Soothe is a trademark of|
Bausch & Lomb Incorporated
or its affiliates.

© 2022 Bausch & Lomb
Incorporated or its affiliates
Product of France

Package/Label Principal Display Panel

carton-3839601

Bausch & Lomb
Soothe®

Lubricant Eye Drops

  PRESERVATIVE FREE

Dry Eye Therapy

 
Moisturizes
 
Comforts
 
Lasts
 
Recommended
for LASIK dryness*
 
30 Single-Use Vials

Sterile 0.02 FL OZ EA (0.6 mL EA)

3839601

SootheEyeDrops.com

Order No. 622219

SOOTHE 
glycerin and propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-495
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN6 mg  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL6 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
WATER (UNII: 059QF0KO0R)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24208-495-2828 in 1 CARTON08/26/201006/30/2022
10.6 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2NDC:24208-495-3030 in 1 CARTON05/01/2020
20.6 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34908/26/2010
Labeler - Bausch & Lomb Incorporated (196603781)
Establishment
NameAddressID/FEIBusiness Operations
Bausch & Lomb Incorporated114406598MANUFACTURE(24208-495)

Revised: 1/2023
Document Id: 3ede1d37-bc07-48b6-9a27-200ecd39c81d
Set id: fef002ea-c4bd-4486-a42e-1bbd9d73d28d
Version: 9
Effective Time: 20230131
 
Bausch & Lomb Incorporated