BLINK TRIPLE CARE- polyethylene glycol 400 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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BLINK® TRIPLE CARE

Drug Facts

Active Ingredient

Polyethylene Glycol 400 0.25%

Purpose

Eye lubricant

Uses

For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun.
For use as a protectant against further irritation or to relieve dryness of the eye.
For use as a lubricant to prevent further irritation or to relieve dryness of the eye.

Warnings

For external use only.
To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
Do not use if product changes color.

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.

Keep out of the reach of children.

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

Directions

Shake well before use.

Instill 1 or 2 drops in the affected eye(s) as needed or as directed by your eye care professional.

Inactive Ingredients

Boric Acid; Castor Oil; PEG 40 Hydrogenated Castor Oil; Potassium Chloride; Purified Water; Sodium Borate; Sodium Chloride; Sodium Chlorite (OcuPure® brand) as a preservative; Sodium Hyaluronate

Other Information

Use only if tape seals on top and bottom flaps are intact.

RETAIN THIS CARTON FOR FUTURE REFERENCE.

PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton

$3 SAVINGS
see inside

New!

blink®
triple care

Dry Eye
Lubricating Eye Drops
Moderate-Severe

3-in-1 Extended Relief

Instantly Soothes
Extra Long-Lasting Hydration
Dual-Action Moisture Seal

0.34 FL OZ (10 mL) STERILE

PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton
BLINK TRIPLE CARE 
polyethylene glycol 400 solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29943-006
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)  
Castor oil (UNII: D5340Y2I9G)  
Polyoxyl 40 hydrogenated castor oil (UNII: 7YC686GQ8F)  
Potassium chloride (UNII: 660YQ98I10)  
Water (UNII: 059QF0KO0R)  
Sodium borate (UNII: 91MBZ8H3QO)  
Sodium chloride (UNII: 451W47IQ8X)  
Sodium chlorite (UNII: G538EBV4VF)  
Hyaluronate sodium (UNII: YSE9PPT4TH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:29943-006-1010 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product05/01/2022
2NDC:29943-006-252.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product05/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34905/01/2022
Labeler - Bausch & Lomb Incorporated (196603781)

Revised: 10/2023
Document Id: 0067a0fe-9b06-4837-9e60-af15cd6bf3c4
Set id: a2b34eb0-001b-4f42-a8cc-c2a0150fafcc
Version: 3
Effective Time: 20231002
 
Bausch & Lomb Incorporated