CVS LUBRICANT EYE DROPS 15ML- propylene glycol liquid

CVS Lubricant Eye Drops 15mL by

Drug Labeling and Warnings

CVS Lubricant Eye Drops 15mL by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Inc., KC Pharmaceuticals, Inc., Daewoo. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Propylene glycol 0.6%

Purpose

Lubricant

Uses

• For the temporary relief of burning and irritaion due to dryness of the eye

Warnings

For external use only.

Do not use

• if this product changes color
• if you are sensative to any ingredient in this product

When using this product

• do not touch tip of container to any surface to avoid contamination
• replace cap after each use

Stop use and ask a doctor if

• you experience eye pain
• changes in vision occur
• redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours

Keep out of reach of children.

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

Directions

• shake well befor using.
• instill 1 or 2 drops in the affected eye(s) as needed.

Other information

• Store at room temperature.

Inactive ingredients

Benzalkonium chloride, boric acid, castor oil, disodium edetate hydrate, polyoxyethylene sorbitan monooleate, potassium chloride, purified water, sodium borate, sodium chloride. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

CVS Lubricant Eye Drops 15mL

CVS Lubricant Eye Drops 15mL twin pack

INGREDIENTS AND APPEARANCE

CVS LUBRICANT EYE DROPS 15ML 
propylene glycol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-446
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)
WATER (UNII: 059QF0KO0R)
CASTOR OIL (UNII: D5340Y2I9G)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
HYDROCHLORIC ACID (UNII: QTT17582CB)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-446-01	1 in 1 BOX	09/20/2019
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 69842-446-02	2 in 1 BOX	09/20/2019
2		15 mL in 1 BOTTLE, DROPPER; 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	09/20/2019

Labeler - CVS Pharmacy, Inc. (062312574)

Registrant - KC Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Business Operations
Daewoo		689046329	manufacture(69842-446) , pack(69842-446) , label(69842-446)