CVS EYEWASH- purified water
CVS

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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CVS Eyewash Kit

Active Ingredient

Purified Water USP 98.577% w/v

Purpose

Eyewash

Use

Use for flushing the eye to remove loose foreign material

Warnings

To avoid contamination, do not touch tip of container to any surface.

Do not reuse.

Once opened, discard.

If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists, consult a doctor.

Obtain immediate medical treatment for all open wounds in or near the eyes.

If solution changes color or becomes cloudy do not use nor, if twist-off Tamper Evident top is broken or missing.

Keep Out of Reach of Children

If Swallowed, get medical help or contact a Poison Control Center right away

Directions

Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle.

Inactive Ingredients

Disodium EDTA

Polyhexanide

Sodium Chloride

Sodium Hydroxide

Sodium Phosphate, Dibasic

Sodium Phosphate, Monobasic

Storage and Handling

Store 36°F-104°F

Use 59°F-86°F

Packaging

box vial

CVS EYEWASH
purified water kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69842-209

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69842-209-12	5 in 1 BOX	10/09/2017	12/05/2021
1	NDC:69842-209-10	1 in 1 VIAL; Type 0: Not a Combination Product

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	1 VIAL	15 mL

Part 1 of 1

A-MED BRAND FIRST AID EYE AND SKIN-RINSE
purified water solution

Product Information
Item Code (Source)	NDC:59276-209
Route of Administration	CUTANEOUS, OPHTHALMIC, TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	98.577 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PHOSPHATE, DIBASIC DODECAHYDRATE (UNII: E1W4N241FO)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
POLIHEXANIDE (UNII: 322U039GMF)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:59276-209-10	15 mL in 1 VIAL; 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	11/01/2013

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part349	10/09/2017	12/05/2021

Labeler - CVS (062312574)

Name	Address	ID/FEI	Business Operations
Establishment
Tender Corporation		064437304	manufacture(69842-209)

Revised: 12/2021

Document Id: d26901a9-079a-9daa-e053-2995a90a70f4

Set id: 5b1e83c8-e3b1-8793-e053-2991aa0ac79e

Version: 6

Effective Time: 20211205

CVS