CVS GENTLE TEARS- dextran 70, hypromellose liquid

CVS Gentle Tears by

Drug Labeling and Warnings

CVS Gentle Tears by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Inc., KC Pharmaceuticals, Inc., Unimed. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Dextran 70 0.1%

Hypromellose 0.3%

Purposes

Lubricant

Lubricant

Use

• temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun

Warnings

For external use only

Do not use

• if this solution changes color or becomes cloudy
• if you are sensitive to any ingredient in this product

When using this product

• to avoid contamination, do not touch tip of container to any surface
• do not reuse
• once opened, discard

Stop use and ask a doctor if

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

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• put 1 or 2 drops in the affected eye(s) as needed

Other information

store at 15°-25°C (59°-77°F)

Inactive ingredients

boric acid, disodium edetate hydrate, potassium chloride, purified water, sodium borate, sodium chloride

CVS Gentle Tears 35ct

INGREDIENTS AND APPEARANCE

CVS GENTLE TEARS 
dextran 70, hypromellose liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-474
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68)	DEXTRAN 70	0.1 g  in 100 mL
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) (HYPROMELLOSE, UNSPECIFIED - UNII:3NXW29V3WO)	HYPROMELLOSE, UNSPECIFIED	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM BORATE (UNII: 91MBZ8H3QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-474-01	35 in 1 BOX	01/01/2020
1		0.4 mL in 1 VIAL, SINGLE-USE; 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	01/01/2020

Labeler - CVS Pharmacy, Inc. (062312574)

Registrant - KC Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Business Operations
KC Pharmaceuticals, Inc.		174450460	pack(69842-474) , label(69842-474)

Establishment
Name	Address	ID/FEI	Business Operations
Unimed		689852052	manufacture(69842-474)