VISINE RED EYE TOTAL COMFORT AND TEARS DRY EYE RELIEF- tetrahydrozoline hcl, polyethylene glycol 400, zinc sulfate 
Johnson & Johnson Consumer Inc.

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Visine Red Eye Total Comfort and Tears Dry Eye Relief

VISINE ® Red Eye Total Comfort Multi-Symptom

Drug Facts

Active ingredient

Polyethylene glycol 400 1%

Tetrahydrozoline HCl 0.05%

Zinc sulfate 0.25%

Purpose

Lubricant

Redness reliever

Astringent

Uses

Warnings

For external use only

Ask a doctor before use if you have narrow angle glaucoma.

When using this product

• some users may experience a brief tingling sensation
• pupils may become enlarged temporarily

• overuse may cause more eye redness

• remove contact lenses before using

• do not use if this solution changes color or becomes cloudy

• do not touch tip of container to any surface to avoid contamination

• replace cap after each use

Stop use and ask a doctor if

• you feel eye pain

• changes in vision occur

• redness or irritation of the eye lasts

• condition worsens or lasts more than 72 hours

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• adults and children 6 years of age and over: put 1 or 2 drops in the affected eye(s) up to 4 times a day

• children under 6 years of age: consult a doctor

• children under 2 years of age: do not use

Other information

Store at 20° to 25°C (68° to 77°F)

Inactive ingredients

benzalkonium chloride, boric acid, edetate disodium, glycerin, hypromellose, purified water, sodium chloride, sodium citrate

Questions?

call toll-free 888-734-7648 or 215-273-8755 (collect)

VISINE ® Dry Eye Relief

Drug Facts

Active ingredient

Polyethylene glycol 400 1%

Purpose

Lubricant

Uses

Warnings

For external use only

When using this product

• remove contact lenses before using

• do not use if this solution changes color or becomes cloudy

• do not touch tip of container to any surface to avoid contamination

• replace cap after each use

Stop use and ask a doctor if

• you feel eye pain

• changes in vision occur

• redness or irritation of the eye lasts

• condition worsens or lasts more than 72 hours

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• adults and children 6 years of age and over: put 1 or 2 drops in the affected eye(s) as needed

• children under 6 years of age: consult a doctor

Other information

Store at room temperature

Inactive ingredients

ascorbic acid, benzalkonium chloride, boric acid, dextrose, disodium phosphate, glycerin, glycine, hypromellose, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium citrate, sodium lactate

Questions?

call toll-free 888-734-7648 or 215-273-8755 (collect)

Distributed by:

JOHNSON & JOHNSON CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - Kit Package

VALUE

MULTI-PACK

VISINE ®

RED EYE

TOTAL COMFORT

MULTI-SYMPTOM

ASTRINGENT / LUBRICANT / REDNESS RELIEVER EYE DROPS

UP TO

10 HRS

COMFORT

ALL-IN ONE RELIEF

From Red, Burning,

Watery, Itchy, Dry, Gritty,

Irritated Eyes

Protects Against

Further Irritation

STERILE

Use products only

as directed.

DRY EYE

RELIEF

LUBRICANT EYE DROPS

MOISTURIZES +

SOOTHES DRY,

GRITTY EYES

Designed to Work

Like Real

Tears

1 BOTTLE: VISINE®

RED EYE TOTAL COMFORT MULTI-SYMPTOM

½ FL OZ (15 mL)

1 BOTTLE: VISINE® DRY EYE RELIEF ½ FL OZ (15 mL)

Visine_01

VISINE RED EYE TOTAL COMFORT AND TEARS DRY EYE RELIEF 
tetrahydrozoline hcl, polyethylene glycol 400, zinc sulfate kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0844
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0844-91 in 1 PACKAGE06/08/2020
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE, DROPPER 15 mL
Part 21 BOTTLE, DROPPER 15 mL
Part 1 of 2
VISINE RED EYE TOTAL COMFORT MULTI-SYMPTOM 
tetrahydrozoline hydrochloride, polyethylene glycol 400, and zinc sulfate, unspecified form solution/ drops
Product Information
Item Code (Source)NDC:69968-0360
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.5 mg  in 1 mL
ZINC SULFATE, UNSPECIFIED FORM (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC SULFATE, UNSPECIFIED FORM2.5 mg  in 1 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 40010 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0360-11 in 1 CARTON
115 mL in 1 BOTTLE, DROPPER; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01804/27/2020
Part 2 of 2
VISINE DRY EYE RELIEF 
polyethylene glycol 400 solution/ drops
Product Information
Item Code (Source)NDC:69968-0363
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 40010 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCINE (UNII: TE7660XO1C)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
DEXTROSE (UNII: IY9XDZ35W2)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
BORIC ACID (UNII: R57ZHV85D4)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0363-11 in 1 CARTON
115 mL in 1 BOTTLE, DROPPER; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01804/27/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01806/08/2020
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 12/2023
Document Id: 0bc0ddb3-a084-b451-e063-6394a90af22b
Set id: 0bc0d6e7-9195-db6b-e063-6294a90aef04
Version: 1
Effective Time: 20231205
 
Johnson & Johnson Consumer Inc.