CARBOXYMETHYLCELLULOSE SODIUM solution/ drops

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)

Available from:

AvPAK

Administration route:

OPHTHALMIC

Prescription type:

OTC DRUG

Therapeutic indications:

Eye lubricant - 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.

Authorization status:

OTC monograph final

Summary of Product characteristics

CARBOXYMETHYLCELLULOSE SODIUM- CARBOXYMETHYLCELLULOSE
SODIUM SOLUTION/ DROPS
AVPAK
----------
CARBOXYMETHYLCELLULOSE SODIUM OPHTHALMIC SOLUTION 0.5%
LUBRICANT EYE DROPS
_ACTIVE INGREDIENT_
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 USE IN THE EYES ONLY
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.
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
_DIRECTIONS_
Instill 1 or 2 drops in the affected eye(s) as needed.
_OTHER INFORMATION_
DO NOT USE IF IMPRINTED SEAL ON CAP IS TORN, BROKEN OR MISSING.
Store at room temperature 15°-30°C (59°-86°F).
RETAIN OUTER CARTON FOR FULL PRODUCT DRUG INFORMATION.
_INACTIVE INGREDIENTS_
Boric acid; calcium chloride; magnesium chloride; potassium chloride;
purified water;
PURITE® (stabilized oxychloro complex); sodium borate; and sodium
chloride. May also
contain hydrochloric acid and/or sodium hydroxide to adjust pH.
_QUESTIONS OR COMMENTS?_
1-855-361-3993
PRINCIPAL DISPLAY PANEL
CARBOXYMETHYLCELLULOSE SODIUM
carboxymethylcellulose sodium solution/ drops
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:50268-068
ROUTE OF ADMINISTRATION
OPHTHALMIC
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII:
K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)
CARBOXYMETHYLCELLULOSE
SODIUM, UNSPECIFIED FORM
5 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
SODIUM CHLORITE (UNII: G538EBV4VF)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ