BLINK NOURISH DRY EYE- glycerin solution/ drops

Blink Nourish Dry Eye by

Drug Labeling and Warnings

Blink Nourish Dry Eye 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 (0.75%)

Purpose

Lubricant

Uses

■ Relieves dryness of the eye.
■ Prevents further irritation.

Warnings

For external use only

Do not use
■ if the pink 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)
■ To preserve the quality of the product, do not leave it in places with high temperatures or direct sunlight such as in a car or near a heater.

Inactive Ingredients

L-arginine (amino acid), calcium chloride, citric acid, cyanocobalamin (Vitamin B12), L-leucine (amino acid), magnesium ascorbyl phosphate (Vitamin C + Magnesium), potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate, sodium hyaluronate, sodium hydroxide, taurine (amino acid), trehalose

Questions or comments?

Call: 1-800-553-5340

Package/Label Principal Display Panel

INGREDIENTS AND APPEARANCE

BLINK NOURISH DRY EYE 
glycerin solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29943-008
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	7.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ARGININE (UNII: 94ZLA3W45F)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CYANOCOBALAMIN (UNII: P6YC3EG204)
LEUCINE (UNII: GMW67QNF9C)
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TAURINE (UNII: 1EQV5MLY3D)
TREHALOSE (UNII: B8WCK70T7I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29943-008-10	1 in 1 CARTON	02/27/2025
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 29943-008-03	10 in 1 TRAY	02/27/2025
2		5 in 1 POUCH
2		0.3 mL in 1 VIAL, SINGLE-USE; 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(29943-008)