מדינה: ארצות הברית
שפה: אנגלית
מקור: 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 GEL AVPAK ---------- CARBOXYMETHYLCELLULOSE SODIUM OPHTHALMIC GEL 1% LUBRICANT EYE GEL _DRUG FACTS_ 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 USE IN THE EYES ONLY. TO AVOID CONTAMINATION, DO NOT TOUCH TIP OF CONTAINER TO ANY SURFACE. REPLACE CAP AFTER USING. 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 THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222). DIRECTIONS Shake well before use. 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. Discard 90 days after opening. 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, sodium borate, sodium chloride. Stabilized Oxychloro Complex 2.5%. May contain hydrochloric acid and/or sodium hydroxide to adjust pH. QUESTIONS OR COMMENTS? 1-855-361-3993 Distributed by: AvKARE Pulaski, TN 38478 Rev. 09/2020 AV 09/2020 CARBOXYMETHYLCELLULOSE SODIUM carboxymethylcellulose sodium gel PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:50268-066 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 BORIC ACID (UNII: R57ZHV85D4 קרא את המסמך השלם