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Nightime Relief Lubricant Eye

Medically reviewed on March 5, 2018

Dosage form: ointment
Ingredients: MINERAL OIL 425mg in 1g, PETROLATUM 533mg in 1g
Labeler: Target Corporation
NDC Code: 11673-575

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.

Active ingredients                                                          Purpose

Mineral oil 42.5%........................................................ Eye Lubricant

White petrolatum 57.3%.............................................. Eye Lubricant

Uses

  • For the temporary relief of burning, irritation, and discomfort due to dryness or the eye or exposure to wind or sun.
  • May be used as a protectant against further irritation

Warnings

  • For external use only.
  • To avoid contamination, do not touch tip of contaainer to any surface. Replace cap after using.

Stop use and ask a doctor if you experience eye pain, changes in vision, continued reness or irritation of the eye, or if the condition worsens or persists more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Pull down the lower lid of the affected eye and apply a small amount (1/4") of ointment to the inside of the eyelid

Other information

  • store away from heat
  • protect from freezing
  • use before expiration date marked on container
  • store at 59°-86° (15°-30°)

Inactive ingredient

lanolin alcohol

DISTRIBUTED BY:

TARGET CORP.

MINNEAPOLIS, MN 55403

MADE IN KOREA

NIGHTIME RELIEF LUBRICANT EYE 
mineral oil, and white petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-575
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINERAL OIL (MINERAL OIL) MINERAL OIL425 mg  in 1 g
PETROLATUM (PETROLATUM) PETROLATUM533 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LANOLIN ALCOHOLS 
Packaging
#Item CodePackage Description
1NDC:11673-575-121 TUBE in 1 BOX
13.5 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34903/05/2015
Labeler - Target Corporation (006961700)

 
Target Corporation

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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