CVS Nighttime Dry-Eye Relief

Manufacturer: CVS Pharmacy, Inc.
Effective date: 2017-11-27
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 22:53:07

Label at a glance#

ProductCVS Nighttime 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 marked on container. Store at 59°-86°F (15°-30°C).

Contacts and useful links#

PhoneLabel contact1-800-SHOP CVS

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 - STOP USE 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 freezing.
Use before expiration date marked on container.
Store at 59°-86°F (15°-30°C).

INACTIVE INGREDIENT SECTION

Inactive ingredient

lanolin alcohol

DOSAGE & ADMINISTRATION SECTION

Distributed by:

CVS Pharmacy, Inc.

One CVS Drive

Woonsocket, RI 02895

CVS.com®

1-800-SHOP CVS

Made in Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
702008	mineral oil 42.5 % / petrolatum 57.3 % Ophthalmic Ointment	PSN	4
702008	mineral oil 0.425 MG/MG / petrolatum 0.573 MG/MG Ophthalmic Ointment	SCD	4
702008	mineral oil 42.5 % / petrolatum, white 57.3 % Ophthalmic Ointment	SY	4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59779-788-35	2022-01-28	C162847	48780-1	d6a99b39-b703-a426-e053-dadaa90af4c2	CVS Nighttime Dry-Eye Relief 0.12oz(NBE Refresh PM)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59779-788-35	CVS Nighttime Dry-Eye Relief	3.5 g in 1 TUBE	OINTMENT	3.5		4
59779-788-35	CVS Nighttime Dry-Eye Relief	1 in 1 BOX	OINTMENT	1		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59779-788	CVS NIGHTTIME DRY-EYE RELIEF (MINERAL OIL, AND WHITE PETROLATUM) OINTMENT [CVS PHARMACY, INC.]	4	Legacy NDC, 2 package rows	20171128_fc1c3dad-edf5-45e7-b9cd-adee08d6bca3.zip

Products#

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

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

CVS Nighttime Dry-Eye Relief
Mineral oil, and White petrolatum
LANOLIN ALCOHOLS
MINERAL OIL
PETROLATUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59779-788	59779-788-35

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
Name	UNII	Kind
LANOLIN ALCOHOLS	884C3FA9HE	IACT
MINERAL OIL	T5L8T28FGP	ACTIB
PETROLATUM	4T6H12BN9U	ACTIB

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
5eff2416-8917-bc38-e053-2991aa0a0617			fc1c3dad-edf5-45e7-b9cd-adee08d6bca3	2017-11-27	Warnings	Exact identifier spl id: 5eff2416-8917-bc38-e053-2991aa0a0617 spl set id: fc1c3dad-edf5-45e7-b9cd-adee08d6bca3

Reported adverse events (FAERS/openFDA)#

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