CARBOXYMETHYLCELLULOSE SODIUM gel

מדינה: ארצות הברית

שפה: אנגלית

מקור: NLM (National Library of Medicine)

מרכיב פעיל:

CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)

זמין מ:

AvPAK

מסלול נתינה (של תרופות):

OPHTHALMIC

סוג מרשם:

OTC DRUG

סממני תרפויטית:

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.

מצב אישור:

OTC monograph final

מאפייני מוצר

CARBOXYMETHYLCELLULOSE SODIUM- CARBOXYMETHYLCELLULOSE SODIUM GEL
AVPAK
----------
CARBOXYMETHYLCELLULOSE SODIUM OPHTHALMIC GEL !% PF
(PRESERVATIVE FREE)
LUBRICANT EYE GEL
_ACTIVE INGREDIENT_
Carboxymethylcellulose sodium 1%
_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.
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.
IF SOLUTION CHANGES COLOR OR BECOMES CLOUDY, DO NOT USE.
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_
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_
Use only if single-use container is intact.
Store at room temperature 15°-30°C (59°-86°F).
RETAIN THIS CARTON FOR FUTURE REFERENCE.
_INACTIVE INGREDIENTS_
Calcium chloride, hydrochloric acid, magnesium chloride, potassium
chloride, puried
water, sodium chloride, sodium hydroxide and sodium lactate.
_QUESTIONS OR COMMENTS?_
1-855-361-3993
PRINCIPAL DISPLAY PANEL
CARBOXYMETHYLCELLULOSE SODIUM
AvPAK
carboxymethylcellulose sodium gel
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:50268-065
ROUTE OF ADMINISTRATION
OPHTHALMIC
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
(CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)
CARBOXYMETHYLCELLULOSE
SODIUM
10 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
S