FDA.reportPublic FDA data

Nightime Relief Lubricant Eye

Manufacturer
Target Corporation
Effective date
2015-03-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:55

Label at a glance#

ProductNightime Relief Lubricant Eye
Active ingredientMINERAL OIL, PETROLATUM
Label structure10 sections

Storage and handling

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients                                                          Purpose

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

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

OTC - PURPOSE SECTION

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 SECTION

Warnings

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

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

INDICATIONS & USAGE SECTION

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

STORAGE AND HANDLING SECTION

Other information

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

INACTIVE INGREDIENT SECTION

Inactive ingredient

lanolin alcohol

DOSAGE & ADMINISTRATION SECTION

DISTRIBUTED BY:

TARGET CORP.

MINNEAPOLIS, MN 55403

MADE IN KOREA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-575-122020-01-31C16284748780-19d75b9cf-f083-f424-e053-dadaa90a57cee92a258b-15ee-491e-b367-5d1be85be8c5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-575-12Nightime Relief Lubricant Eye3.5 g in 1 TUBEOINTMENT3.51
11673-575-12Nightime Relief Lubricant Eye1 in 1 BOXOINTMENT11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-575NIGHTIME RELIEF LUBRICANT EYE (MINERAL OIL, AND WHITE PETROLATUM) OINTMENT [TARGET CORPORATION]1Legacy NDC, 2 package rows20150310_e92a258b-15ee-491e-b367-5d1be85be8c5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MINERAL OILACTIVE INGREDIENTT5L8T28FGP1
PETROLATUMACTIVE INGREDIENT4T6H12BN9U1
MINERAL OILACTIVE MOIETYT5L8T28FGP1
PETROLATUMACTIVE MOIETY4T6H12BN9U1
LANOLIN ALCOHOLSINACTIVE INGREDIENT884C3FA9HE1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-57511673-575-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
MINERAL OILT5L8T28FGPACTIB
PETROLATUM4T6H12BN9UACTIB
LANOLIN ALCOHOLS884C3FA9HEIACT

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LANOLIN ALCOHOLSLANOLIN ALCOHOLS884C3FA9HEOINTMENT / TOPICAL452 mgExact identifier — unii candidate
4 equally ranked IID candidates
LANOLIN ALCOHOLSLANOLIN ALCOHOLS884C3FA9HECREAM / TOPICAL6 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
LANOLIN ALCOHOLSLANOLIN ALCOHOLS884C3FA9HEOINTMENT / OPHTHALMIC10 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
LANOLIN ALCOHOLSLANOLIN ALCOHOLS884C3FA9HELOTION / TOPICAL9360 mgExact identifier — unii candidate
4 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c8c23d33-f56c-4cae-b373-cbae4459c0f8e92a258b-15ee-491e-b367-5d1be85be8c52015-03-05WarningsExact identifier
spl id: c8c23d33-f56c-4cae-b373-cbae4459c0f8
spl set id: e92a258b-15ee-491e-b367-5d1be85be8c5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.