País: Estados Unidos
Língua: inglês
Origem: NLM (National Library of Medicine)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)
AvPAK
OPHTHALMIC
OTC DRUG
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.
OTC monograph final
CARBOXYMETHYLCELLULOSE SODIUM- CARBOXYMETHYLCELLULOSE SODIUM SOLUTION/ DROPS AVPAK ---------- CARBOXYMETHYLCELLULOSE SODIUM OPHTHALMIC SOLUTION 0.5% (PRESERVATIVE FREE) 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. TO AVOID CONTAMINATION, DO NOT TOUCH TIP OF CONTAINER TO ANY SURFACE. DO NOTREUSE. 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 (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_ 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; purified water; sodium chloride; sodium hydroxide and sodium lactate. _QUESTIONS OR COMMENTS?_ 1-855-361-3993 PRINCIPAL DISPLAY PANEL CARBOXYMETHYLCELLULOSE SODIUM carboxymethylcellulose sodium solution/ drops PRODUCT INFORMATION AvPAK PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:50268-067 ROUTE OF ADMINISTRATION OPHTHALMIC ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM 5 mg in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH CALCIUM CHLORIDE (UNII: M4I0D6VV5M) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM Leia o documento completo