EQUATE RESTORE PLUS LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops
Walmart, 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 Restore Plus 70 Ct., PLD

Active ingredients

Carboxymethylcellulose sodium 0.5%

Purpose

Carboxymethylcellulose sodium.....Lubricant

Uses

for the temporary relief of burning, irritation, and discomfort due to dryness of the eyes or exposure to wind or sun
may be used as a protectant against further irritation

Warnings

For external use only

Do not use this product if

solution changes color or becomes cloudy

When using this product

do not reuse
once opened, discard
to avoid contamination, do not touch tip of container to any surface
do not touch unit-dose tip to eye

Stop use and ask a doctor if

you experience eye pain
changes in vision occur
redness or irritation of the eye continues
redness or irritation of the eye worsens or persists for more than 72 hours

Keep out of the reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

to open, twist and pull tab to remove
instill 1 or 2 drops in the affected eye(s) as needed and discard container
if used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor’s instructions

Other information

store at 15°-25°C (59°-77°F)
use only if single-use container is intact
use before expiration date marked on container
RETAIN THIS CARTON FOR FUTURE REFERENCE

Inactive ingredients calcium chloride, **hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate. **May contain these ingredients to adjust pH.

Questions or comments? Call 1-888-287-1915

carton

EQUATE RESTORE PLUS LUBRICANT EYE DROPS
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-389
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	0.5 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
SODIUM LACTATE (UNII: TU7HW0W0QT)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:49035-389-01	70 in 1 CARTON	03/04/2022
1		0.4 mL in 1 VIAL, SINGLE-USE; 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	03/04/2020

Labeler - Walmart, Inc. (051957769)

Registrant - K.C. Pharmaceuticals, Inc. (174450460)

Name	Address	ID/FEI	Business Operations
Establishment
K.C. Pharmaceuticals, Inc.		174450460	pack(49035-389) , label(49035-389)

Name	Address	ID/FEI	Business Operations
Establishment
Unimed Pharmaceuticals, Inc.		689852052	manufacture(49035-389)

Revised: 4/2020

Document Id: a37194c5-227f-9de6-e053-2995a90a222f

Set id: 9e665ca2-4fa6-fdb4-e053-2a95a90abcca

Version: 4

Effective Time: 20200416

Walmart, Inc.