Nighttime Dry-Eye Relief

Manufacturer
CVS
Effective date
2019-08-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:00:34

Label at a glance#

ProductNighttime Dry-Eye Relief
Active ingredientMINERAL OIL, PETROLATUM
Label structure10 sections

Storage and handling

Other information store away from heat protect from freezing use before expiration date on the tube 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 container to any surface.
  • Keep tube tightly closed.

OTC - STOP USE SECTION

Stop use and ask a doctor if:

  • You experience eye pain, changes in vision, continued redness or irritation of the eye.
  • The condition worsens or persists for 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 at 1-800-222-1222.

INDICATIONS & USAGE SECTION

Directions

• Wash your hands.
• Pull down the lower lid of the affected eye and gently 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 on the tube
  • store at 59°-86° (15°-30°)

INACTIVE INGREDIENT SECTION

Inactive ingredient

lanolin alcohol

DOSAGE & ADMINISTRATION SECTION

Directions

• Wash your hands.
• Pull down the lower lid of the affected eye and gently apply a small amount (1/4”) of ointment to the inside of the eyelid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
702008mineral oil 42.5 % / petrolatum 57.3 % Ophthalmic OintmentPSN1
702008mineral oil 0.425 MG/MG / petrolatum 0.573 MG/MG Ophthalmic OintmentSCD1
702008mineral oil 42.5 % / petrolatum, white 57.3 % Ophthalmic OintmentSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69842-568-132021-01-29C16284748780-1ba0f9c33-28b1-a910-e053-dadaa90a0b85Nighttime Dry-Eye Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-568-13Nighttime Dry-Eye Relief1 in 1 BOXOINTMENT11
69842-568-13Nighttime Dry-Eye Relief3.5 g in 1 TUBEOINTMENT3.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-568NIGHTTIME DRY-EYE RELIEF (MINERAL OIL, AND WHITE PETROLATUM) OINTMENT [CVS]1Legacy NDC, 2 package rows20190926_92ba5957-e5df-1a75-e053-2a95a90ad475.zip

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
69842-56869842-568-13

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
LANOLIN ALCOHOLS884C3FA9HEIACT
MINERAL OILT5L8T28FGPACTIB
PETROLATUM4T6H12BN9UACTIB

Source Document#

Source XML

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
92ba5957-e5e0-1a75-e053-2a95a90ad47592ba5957-e5df-1a75-e053-2a95a90ad4752019-08-30WarningsExact identifier
spl id: 92ba5957-e5e0-1a75-e053-2a95a90ad475
spl set id: 92ba5957-e5df-1a75-e053-2a95a90ad475

Reported adverse events (FAERS/openFDA)#

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