BLINK TEARS- polyethylene glycol 400 solution/ drops 
Bausch & Lomb Incorporated

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Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Polyethylene Glycol 400 0.25%

Purpose

Eye lubricant

Uses

WARNINGS

Stop use and ask 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other Information

INACTIVE INGREDIENT SECTION

Boric Acid, Calcium Chloride, Magnesium Chloride, Potassium Chloride, Purified Water, Sodium Borate, Sodium Chloride, Sodium Hyaluronate.

OTC - QUESTIONS SECTION

In the U.S. call 1-800-347-5005

www.yourhealthyeyes.com

PRINCIPAL DISPLAY PANEL - 5 Vial Carton

PRESERVATIVE FREE

blink ®
tears

Dry Eye
Lubricating Eye Drops
Mild-Moderate

5 STERILE
Single-Use Vials

Long-Lasting Relief

Instantly Soothes & Hydrates
PROFESSIONAL SAMPLE - NOT FOR RESALE

0.01 FL OZ (0.4 mL) EACH

PRINCIPAL DISPLAY PANEL - 5 Vial Carton

PRINCIPAL DISPLAY PANEL - 25 Vial Carton

PRESERVATIVE FREE

Immediate
Relief

blink ®
tears

Dry Eye
Lubricating Eye Drops
Mild-Moderate

Long-Lasting Relief

Instantly Soothes & Hydrates

0.01 FL OZ (0.4 mL) EACH

25
STERILE
Single-Use
Vials

PRINCIPAL DISPLAY PANEL - 25 Vial Carton

PRINCIPAL DISPLAY PANEL - 180 Vial Carton

1 packer = 36 strips (180 vials)

Professional use - Not for resale

THIS SIDE UP

No. 94153
Store away from heat
Protect from freezing

Blink ®Tears Lubricating Eye Drops
0.01 fl oz (0.4 mL)
40171-00536

Product of Germany

Blink is a trademark of
Johnson & Johnson
Surgical Vision, Inc.

© Johnson & Johnson Surgical Vision, Inc. 2023
Johnson & Johnson Surgical Vision, Inc.
Irvine, CA 92618 U.S.A.
1-800-347-5005

PRINCIPAL DISPLAY PANEL - 180 Vial Carton
BLINK TEARS 
polyethylene glycol 400 solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:40171-005
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4002.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:40171-005-055 in 1 CARTON03/15/2016
10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2NDC:40171-005-2525 in 1 CARTON03/15/2016
20.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
3NDC:40171-005-36180 in 1 CARTON03/23/2016
30.4 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 DrugM01803/15/2016
Labeler - Bausch & Lomb Incorporated (196603781)

Revised: 9/2024
Document Id: 2298793e-fe31-cd2b-e063-6394a90ad92b
Set id: 10fcf407-6eaf-4730-9ed0-9b7715cf5701
Version: 10
Effective Time: 20240920
 
Bausch & Lomb Incorporated