EQUATE EYE DROPS DRY EYE RELIEF- glycerin, hypromellose, polyethylene glycol 400 liquid
Wal-Mart Stores, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Equate Dry Eye Relief Eye Drops 15mL - 2 pack

Active ingredients

Glycerin 0.2%

Hypromellose 0.2%

Polyethylene glycol 400 1%

Purposes

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 Dry Eye Relief Eye Drops 2-0.5oz bottles

Equate Eye Drops Dry Eye Relief 2-0.5oz bottles

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.2 g in 100 mL
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

Ingredient Name	Strength
Inactive Ingredients
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
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
2	NDC:49035-280-02	2 in 1 BOX	02/01/2021
2		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part349	11/01/2019

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

Registrant - KC Pharmaceuticals, Inc. (174450460)

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

Revised: 12/2022

Document Id: efe2d9bf-46ad-9687-e053-2a95a90a6e79

Set id: 91fb8fb5-b871-4535-e053-2995a90a9b16

Version: 5

Effective Time: 20221215

Wal-Mart Stores, Inc.