BLINK TRIPLE CARE- polyethylene glycol 400 solution/ drops

BLINK TRIPLE CARE by

Drug Labeling and Warnings

BLINK TRIPLE CARE by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Surgical Vision, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Polyethylene glycol 400 0.25%

Purpose

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

Do not use

• if product changes color

  When using this product

• to avoid contamination, do not touch tip of container to any surface
• replace cap after each use

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 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.

Other Information

• Store at 15-25 °C (59-77 °F)
• RETAIN THIS CARTON FOR FUTURE REFERENCE

Inactive Ingredients

boric acid; castor oil; PEG 40 hydrogenated castor oil; potassium chloride; purified water; sodium borate; sodium chloride; sodium chlorite as a preservative; sodium hyaluronate.

Questions or comments?

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PRINCIPAL DISPLAY PANEL

BAUSCH + LOMB

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

INGREDIENTS AND APPEARANCE

BLINK TRIPLE CARE 
polyethylene glycol 400 solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29943-006
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	2.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29943-006-10	10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/01/2022
2	NDC: 29943-006-25	2.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	05/01/2022

Labeler - Bausch & Lomb Incorporated (196603781)

Establishment
Name	Address	ID/FEI	Business Operations
Bausch & Lomb Incorporated Greenville, South Carolina		114406598	manufacture(29943-006)