EQUATE EYE DROPS DRY EYE RELIEF- glycerin, hypromellose, polyethylene glycol 400 liquid

Equate Eye Drops Dry Eye Relief by

Drug Labeling and Warnings

Equate Eye Drops Dry Eye Relief by is a Otc medication manufactured, distributed, or labeled by Wal-Mart Stores, Inc., KC Pharmaceuticals, Inc., KC Pharmaceutical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Glycerin 0.2%

Hypromellose 0.2%

Polyethylene glycol 400 1%

Purposes

Lubricant

Lubricant

Lubricant

Uses

• for protection against further irritation
• for temporary relief of burning and irritation due to dryness of the eye

Warnings

For external use only

Do not use this product if

solution changes color or becomes cloudy

When using this product

• to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
• remove contact lenses before using

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 for 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

instill 1 to 2 drops in the affected eye(s) as needed

Other information

store at 15°-30°C (59°-86°F)

Inactive ingredients

benzalkonium chloride, dextrose, edetate disodium, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate, sodium phosphate dibasic, sodium phosphate monobasic

Questions or comments?

1-888-287-1915

Equate Eye Drops Dry Eye Relief

INGREDIENTS AND APPEARANCE

EQUATE EYE DROPS DRY EYE RELIEF 
glycerin, hypromellose, polyethylene glycol 400 liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-280
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) (HYPROMELLOSE, UNSPECIFIED - UNII:3NXW29V3WO)	HYPROMELLOSE, UNSPECIFIED	0.2 g  in 100 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL, UNSPECIFIED - UNII:3WJQ0SDW1A)	POLYETHYLENE GLYCOL 400	1 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
DEXTROSE (UNII: IY9XDZ35W2)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49035-280-01	2 in 1 BOX	11/01/2019
1		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	11/01/2019

Labeler - Wal-Mart Stores, Inc. (051957769)

Registrant - KC Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Business Operations
KC Pharmaceutical, Inc.		174450460	manufacture(49035-280) , pack(49035-280) , label(49035-280)