CVS LUBRICANT EYE DROPS- carboxymethylcellulose sodium liquid

United States - English - NLM (National Library of Medicine)

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Active ingredient:
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)
Available from:
CVS Pharmacy, Inc.
Administration route:
OPHTHALMIC
Prescription type:
OTC DRUG
Therapeutic indications:
Lubricant - 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
Authorization status:
OTC monograph final
Authorization number:
69842-804-01

CVS LUBRICANT EYE DROPS- carboxymethylcellulose sodium liquid

CVS Pharmacy, 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.

----------

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpos e

Lubricant

Us es

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, magnesium chloride, potassium chloride, purified water, sodium chloride and sodium

lactate. May contain sodium hydroxide and/or hydrochloric acid to adjust pH.

CVS Lubricant Eye Drops Preservative Free 70 ct

CVS LUBRICANT EYE DROPS

carboxymethylcellulose sodium liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:6 9 8 42-8 0 4

Route of Administration

OPHTHALMIC

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

CARBO XYMETHYLCELLULO SE SO DIUM (UNII: K6 79 OBS311)

(CARBOXYMETHYLCELLULOSE - UNII:0 5JZI7B19 X)

CARBOXYMETHYLCELLULOSE

SODIUM

0 .5 g

in 10 0 mL

Inactive Ingredients

Ingredient Name

Stre ng th

SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)

SO DIUM LACTATE (UNII: TU7HW0 W0 QT)

SO DIUM HYDRO XIDE (UNII: 55X0 4QC32I)

MAGNESIUM CHLO RIDE (UNII: 0 2F3473H9 O)

PO TASSIUM CHLO RIDE (UNII: 6 6 0 YQ9 8 I10 )

HYDRO CHLO RIC ACID (UNII: QTT1758 2CB)

CALCIUM CHLO RIDE (UNII: M4I0 D6 VV5M)

WATER (UNII: 0 59 QF0 KO0 R)

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:6 9 8 42-8 0 4-

70 in 1 BOX

0 7/30 /20 19

1

0 .4 mL in 1 VIAL, SINGLE-USE; Type 0 : No t a Co mbinatio n

Pro duc t

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph final

pa rt349

0 7/30 /20 19

Labeler -

CVS Pharmacy, Inc. (062312574)

Registrant -

KC Pharmaceuticals, Inc. (174450460)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

KC Pharmaceuticals, Inc.

174450 46 0

pack(6 9 8 42-8 0 4) , label(6 9 8 42-8 0 4)

CVS Pharmacy, Inc.

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Unimed

6 8 9 8 520 52

ma nufa c ture (6 9 8 42-8 0 4)

Revised: 7/2019

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