VISINE DRY EYE RELIEF- glycerin, hypromelloses, and polyethylene glycol 400 solution/ drops 
Johnson & Johnson Consumer Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Visine® Dry Eye Relief Formula

Drug Facts

Active ingredientsPurpose
Glycerin 0.2%Lubricant
Hypromellose 0.2%Lubricant
Polyethylene glycol 400 1%Lubricant

Use

  • for the temporary relief of burning and irritation due to dryness of the eye
  • for protection against further irritation

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

  • put 1 to 2 drops in the affected eye(s) as needed
  • children under 6 years of age: ask a doctor

Other information

  • store at 15° to 25°C (59° to 77°F)

Inactive ingredients

Ascorbic Acid, Benzalkonium Chloride, Boric Acid, Dextrose, Disodium Phosphate, Glycine, 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)

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton

Sterile
Visine®

DRY EYE
Relief
LUBRICANT EYE DROPS

Relieves
burning,
gritty,
irritated
DRY EYES

1/2 FL. OZ. (15 mL)

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton
VISINE DRY EYE RELIEF 
glycerin, hypromelloses, and polyethylene glycol 400 solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42002-210
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Glycerin (UNII: PDC6A3C0OX) (Glycerin - UNII:PDC6A3C0OX) Glycerin2 mg  in 1 mL
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) (HYPROMELLOSE, UNSPECIFIED - UNII:3NXW29V3WO) HYPROMELLOSE, UNSPECIFIED2 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
Ascorbic Acid (UNII: PQ6CK8PD0R)  
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
Boric Acid (UNII: R57ZHV85D4)  
Dextrose, Unspecified Form (UNII: IY9XDZ35W2)  
Sodium Phosphate, Dibasic, Anhydrous (UNII: 22ADO53M6F)  
Glycine (UNII: TE7660XO1C)  
Magnesium Chloride (UNII: 02F3473H9O)  
Potassium Chloride (UNII: 660YQ98I10)  
Water (UNII: 059QF0KO0R)  
Sodium Borate (UNII: 91MBZ8H3QO)  
Sodium Chloride (UNII: 451W47IQ8X)  
Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR)  
Sodium Lactate (UNII: TU7HW0W0QT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:42002-210-051 in 1 CARTON06/05/200906/01/2021
115 mL in 1 BOTTLE, DROPPER; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
2NDC:42002-210-022 in 1 CARTON06/05/200906/01/2021
2NDC:42002-210-051 in 1 CARTON
215 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 FINALpart34906/05/200906/01/2021
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 1/2020
Document Id: 9c9ebf9f-782d-4a6e-bb55-5e8b79a8992c
Set id: 7a34cecf-1fbc-4af7-894f-a4362f2eed58
Version: 4
Effective Time: 20200106
 
Johnson & Johnson Consumer Inc.