Walgreens Sterile Lubricant Eye

Manufacturer
Walgreen Company
Effective date
2015-09-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:43:38

Label at a glance#

ProductWalgreens Sterile Lubricant Eye
Active ingredientMINERAL OIL, PETROLATUM
Label structure10 sections

Storage and handling

Other information Store away from heat. Protect from feezing. Use before expiration date marked on container. Store at 59° to 86°F (15° to 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 of 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 container to any surface. Replace cap after using.

OTC - ASK DOCTOR SECTION

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 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 feezing.
  • Use before expiration date marked on container.
  • Store at 59° to 86°F (15° to 30°)

INACTIVE INGREDIENT SECTION

Inactive ingredient

lanolin alcohol

DOSAGE & ADMINISTRATION SECTION

Distributed by:

Walgreen Co.

200 Milmot Rd.

Deerfield, IL 60015

Made in Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
702008mineral oil 42.5 % / petrolatum 57.3 % Ophthalmic OintmentPSN2
702008mineral oil 0.425 MG/MG / petrolatum 0.573 MG/MG Ophthalmic OintmentSCD2
702008mineral oil 42.5 % / petrolatum, white 57.3 % Ophthalmic OintmentSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130311917177274GTIN-13: 0311917177274
EAN-13: 0311917177274
GTIN-12: 311917177274
UPC-A: 311917177274
GTIN storage (14 digits): 00311917177274
905296.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-7274-122020-01-31C16284748780-19d75b9d0-7a2f-f424-e053-dadaa90a57ce6bb68dc4-da71-4134-9ec4-9c4faecb3b88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-7274-12Walgreens Sterile Lubricant Eye3.5 g in 1 TUBEOINTMENT3.52
0363-7274-12Walgreens Sterile Lubricant Eye1 in 1 CARTONOINTMENT12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-7274WALGREENS STERILE LUBRICANT EYE (MINERAL OIL, AND WHITE PETROLATUM) OINTMENT [WALGREEN COMPANY]2Legacy NDC, 2 package rows20150921_6bb68dc4-da71-4134-9ec4-9c4faecb3b88.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-7274-12GM - Gram0363-7274333613ec-ef8e-4bf2-977d-b98a51e6968d12020-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MINERAL OILACTIVE INGREDIENTT5L8T28FGP2
PETROLATUMACTIVE INGREDIENT4T6H12BN9U2
MINERAL OILACTIVE MOIETYT5L8T28FGP2
PETROLATUMACTIVE MOIETY4T6H12BN9U2
LANOLIN ALCOHOLSINACTIVE INGREDIENT884C3FA9HE2

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
0363-72740363-7274-12

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

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 ALCOHOLS884C3FA9HECREAM / TOPICAL6 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
LANOLIN ALCOHOLSLANOLIN ALCOHOLS884C3FA9HELOTION / TOPICAL9360 mgExact identifier — unii candidate
4 equally ranked IID candidates
LANOLIN ALCOHOLSLANOLIN ALCOHOLS884C3FA9HEOINTMENT / OPHTHALMIC10 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
LANOLIN ALCOHOLSLANOLIN ALCOHOLS884C3FA9HEOINTMENT / TOPICAL452 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
406606f3-9aec-492e-9e13-8d58be6ea6cc6bb68dc4-da71-4134-9ec4-9c4faecb3b882015-09-21WarningsExact identifier
spl id: 406606f3-9aec-492e-9e13-8d58be6ea6cc
spl set id: 6bb68dc4-da71-4134-9ec4-9c4faecb3b88

Reported adverse events (FAERS/openFDA)#

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