BLINK BOOST- glycerin solution/ drops

blink boost by

Drug Labeling and Warnings

blink boost by is a Otc medication manufactured, distributed, or labeled by Bausch & Lomb Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Glycerin (0.5%)

Purpose

Lubricant

Uses

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

Warnings

For external use only

Do not use
■ if solution changes color or becomes cloudy
■ if tamper evident ring is broken or missing

When using this product
■ do not touch tip of container to any surface to avoid contamination
■ replace cap after using

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

■ remove tamper evident ring, then remove cap
■ tip bottle at a downward angle or upside down (to deliver drop to eye)
■ squeeze bottle to instill 1 or 2 drops in the affected eye(s) as needed
■ replace cap after use

Other information

■ store at 15–25 °C (59–77 °F)

Inactive Ingredients

boric acid, erythritol, potassium chloride, purified water, sodium borate, sodium hyaluronate

Questions or comments?

Call: 1-800-553-5340

Package/Label Principal Display Panel

INGREDIENTS AND APPEARANCE

BLINK BOOST 
glycerin solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29943-007
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
ERYTHRITOL (UNII: RA96B954X6)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29943-007-05	1 in 1 CARTON	02/27/2025
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	02/27/2025

Labeler - Bausch & Lomb Incorporated (196603781)

Establishment
Name	Address	ID/FEI	Business Operations
Bausch & Lomb Incorporated		114406598	manufacture(29943-007)