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

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

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)