NIGHTTIME DRY-EYE RELIEF- mineral oil, and white petrolatum ointment

Nighttime Dry-Eye Relief by

Drug Labeling and Warnings

Nighttime Dry-Eye Relief by is a Otc medication manufactured, distributed, or labeled by CVS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients Purpose

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

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

PURPOSE

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

Warnings

• For external use only.
• To avoid contamination, do not touch tip of container to any surface.
• Keep tube tightly closed.

STOP USE

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. .

KEEP OUT OF REACH OF CHILDREN

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

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

Other information

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

INACTIVE INGREDIENT

Inactive ingredient

lanolin alcohol

DOSAGE & ADMINISTRATION

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NIGHTTIME DRY-EYE RELIEF 
mineral oil, and white petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-568
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP)	MINERAL OIL	425 mg  in 1 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	573 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-568-13	1 in 1 BOX	08/30/2019
1		3.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	08/30/2019

Labeler - CVS (062312574)