SUNMARK LUBRICATING PLUS- carboxymethylcellulose sodium solution/ drops 
Strategic Sourcing Services LLC

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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McKesson Lubricating Plus Eye Drops Drug Facts

Active ingredient (in each single-use container)

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

Uses

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

Warnings

For external use only

Do not use

if solution changes color or becomes cloudy

When using this product

to avoid contamination

do not touch tip of container to any surface
do not reuse
once opened, discard
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 reach of children.

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

Directions

to open, twist and pull tab to remove
instill 1 or 2 drops in the affected eye(s) as needed and discard container

Other information

store at 20-25°C (68-77°F)
RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

calcium chloride dihydrate, magnesium chloride hexahydrate, potassium chloride, sodium chloride, sodium lactate solution, water for injection. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

sunmark®

COMPARE TO REFRESH PLUS® ACTIVE INGREDIENT

lubricating plus

Carboxymethylcellulose Sodium 0.5%

Lubricant Eye Drops

Moisturizing Relief

Sterile

PRESERVATIVE FREE

Actual vial size

30 Sterile Single-Use Containers

0.01 FL OZ (0.4 mL) EACH

lubricating plus image
SUNMARK LUBRICATING PLUS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-329
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49348-329-446 in 1 CARTON06/06/2013
15 in 1 POUCH
10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34906/06/2013
Labeler - Strategic Sourcing Services LLC (116956644)

Revised: 11/2022
Document Id: af196572-2edf-44ca-9fa8-920f14205820
Set id: 043ea5ed-be47-4824-94ee-9b6004f079f7
Version: 5
Effective Time: 20221117
 
Strategic Sourcing Services LLC