FDA.reportPublic FDA data

REFRESH ® LACRI-LUBE ® Drug Facts

Manufacturer
Allergan, Inc.
Effective date
2026-05-15
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:58:16

Label at a glance#

ProductREFRESH LACRI-LUBE
Active ingredientMINERAL OIL, PETROLATUM
Label structure9 sections

Indications and 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.

Dosage and administration

Pull down the lower lid of the affected eye and apply a small amount (one-fourth inch) of ointment to the inside of the eyelid.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Mineral Oil 42.5%

White Petrolatum 56.8%

Purpose

OTC - PURPOSE SECTION

Eye lubricant

Eye lubricant

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

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.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Pull down the lower lid of the affected eye and apply a small amount (one-fourth inch) of ointment to the inside of the eyelid.

Other information

OTHER SAFETY INFORMATION

  • Store away from heat.
  • Protect from freezing.
  • Use only if tape seals on top and bottom flaps are intact.
  • Use before expiration date marked on container.
  • Store at 59°-77°F (15°-25°C).
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Chlorobutanol and Lanolin alcohols.

Questions or comments?

OTC - QUESTIONS SECTION

1.800.678.1605

refresheyedrops.com

v2.0DFL0312

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0023-0312-04

Refresh®

LACRI-LUBE®

Lubricant Eye Ointment

DOCTOR#1 RECOMMENDED 

Nighttime Relief

For Intense Dry Eyes

Net wt. 0.12 oz (3.5 g) Sterile

Principal Display Panel NDC 0023-0312-04 Refresh® LACRI-LUBE® Lubricant Eye Ointment DOCTOR#1 RECOMMENDEDNighttime Relief For Intense Dry Eyes Net wt. 0.12 oz (3.5 g) SterilePrincipal Display Panel NDC 0023-0312-04 Refresh® LACRI-LUBE® Lubricant Eye Ointment DOCTOR#1 RECOMMENDEDNighttime Relief For Intense Dry Eyes Net wt. 0.12 oz (3.5 g) Sterile

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
701984mineral oil 42.5 % / petrolatum 56.8 % Ophthalmic OintmentPSN8
701984mineral oil 0.425 MG/MG / petrolatum 0.568 MG/MG Ophthalmic OintmentSCD8
701984mineral oil 42.5 % / petrolatum, white 56.8 % Ophthalmic OintmentSY8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0023-0312-04REFRESH LACRI-LUBE1 in 1 CARTONOINTMENT18
0023-0312-04REFRESH LACRI-LUBE3.5 g in 1 TUBEOINTMENT3.58
0023-0312-07REFRESH LACRI-LUBE1 in 1 CARTONOINTMENT18
0023-0312-07REFRESH LACRI-LUBE7 g in 1 TUBEOINTMENT78

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0023-0312-04GM - Gram0023-031220b39866-d70e-43a9-aba4-f2788fd84ed812012-07-24
0023-0312-07GM - Gram0023-0312908fe98b-82bb-4d73-892c-9c93a24b96d612012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
mineral oilACTIVE INGREDIENTT5L8T28FGP2
petrolatumACTIVE INGREDIENT4T6H12BN9U2
mineral oilACTIVE MOIETYT5L8T28FGP2
petrolatumACTIVE MOIETY4T6H12BN9U2
chlorobutanolINACTIVE INGREDIENTHM4YQM8WRC2
lanolin alcoholsINACTIVE INGREDIENT884C3FA9HE2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0023-03120023-0312-04, 0023-0312-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
MINERAL OILT5L8T28FGPACTIB
PETROLATUM4T6H12BN9UACTIB
CHLOROBUTANOLHM4YQM8WRCIACT
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 · 6 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
lanolin alcoholsLANOLIN ALCOHOLS884C3FA9HEOINTMENT / OPHTHALMIC10 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates
chlorobutanolCHLOROBUTANOLHM4YQM8WRCOINTMENT / OPHTHALMIC0.65 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates
chlorobutanolCHLOROBUTANOLHM4YQM8WRCOINTMENT / OPHTHALMIC0.65 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates
lanolin alcoholsLANOLIN ALCOHOLS884C3FA9HEOINTMENT / OPHTHALMIC10 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates
chlorobutanolCHLOROBUTANOLHM4YQM8WRCOINTMENT / OPHTHALMIC0.65 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates
lanolin alcoholsLANOLIN ALCOHOLS884C3FA9HEOINTMENT / OPHTHALMIC10 %w/wExact identifier — unii+route+dosage form
3 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
REFRESH LACRI-LUBEMINERAL OIL, PETROLATUMAllergan, Inc.d232a44b-516d-4cdf-a4e7-c3a9a50dc7af2026-05-15WarningsExact identifier
ndc (package): 0023-0312-07
ndc (package): 0023-0312-04
ndc (product): 0023-0312
ndc11 (package): 00023031207
ndc11 (package): 00023031204
spl id: b6d64a52-8a8a-4c90-ac67-41a32cc3c78a
spl set id: d232a44b-516d-4cdf-a4e7-c3a9a50dc7af

Reported adverse events (FAERS/openFDA)#

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