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Dry eye relief by McKesson Corporation

Dosage form: liquid
Ingredients: HYPROMELLOSES 0.2g in 100mL, GLYCERIN 0.2g in 100mL, POLYETHYLENE GLYCOL 400 1g in 100mL
Labeler: McKesson Corporation
NDC Code: 49348-095

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.

DRUG FACTS

​Active ingredients

Glycerin 0.2%

Hypromellose 0.2%

Polyethylene glycol 1%

​Purpose

Glycerin.....Lubricant

Hypromellose.....Lubricant

Polyethylene glycol 400.....Lubricant

​Uses

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

​Warnings

For external use only

Do not use this product if solution changes color or becomes cloudy

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

When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • replace cap after using. Keep container tightly closed
  • remove contact lens before using

Keep out of reach of children

If accidentally swallowed get medical help or contact a Poison Control Center immediately

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

Directions

  • Instill 1 or 2 drops in the affected eye(s) as needed
  • Children under 6 years of age: ask doctor

Other information

RETAIN THIS CARTON FOR FUTURE REFERENCE

Store at 15oC-30oC (59o-86oF)

​Inactive ingredients

dextrose, sodium chloride, potassium chloride, sodium phosphate monobasic, sodium phosphate dibasic, sodium bicarbonate, sodium citrate, edetate disodium, benzalkonium chloride, purified water

DRY EYE RELIEF 
glycerin, hypromellose, polyethylene glycol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-095
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPROMELLOSES (HYPROMELLOSE, UNSPECIFIED) HYPROMELLOSES0.2 g  in 100 mL
GLYCERIN (GLYCERIN) GLYCERIN0.2 g  in 100 mL
POLYETHYLENE GLYCOL 400 (POLYETHYLENE GLYCOL 400) POLYETHYLENE GLYCOL 4001 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
DEXTROSE 
SODIUM CHLORIDE 
SODIUM PHOSPHATE, MONOBASIC 
POTASSIUM CHLORIDE 
SODIUM PHOSPHATE, DIBASIC 
SODIUM BICARBONATE 
SODIUM CITRATE 
EDETATE DISODIUM 
BENZALKONIUM CHLORIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:49348-095-291 BOTTLE, PLASTIC in 1 CARTON
115 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34905/01/2013
Labeler - McKesson Corporation (177667227)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIOperations
KC Pharmaceuticals, Inc.174450460manufacture(49348-095), pack(49348-095), label(49348-095)

Revised: 02/2017
 
McKesson Corporation

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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