מדינה: ארצות הברית
שפה: אנגלית
מקור: NLM (National Library of Medicine)
Hypromellose 2910 (4000 Mpa.s) (UNII: RN3152OP35) (Hypromellose 2910 (4000 Mpa.s) - UNII:RN3152OP35)
OCuSOFT, Inc.
Hypromellose 2910 - UNII:RN3152OP35)
Hypromellose 2910 (4000 Mpa.s) 3 mg in 1 mL
OPHTHALMIC
OTC DRUG
Warnings ▪ For use in the eyes only. When using this product ▪ do not touch tip of container to any surface to avoid contamination. ▪ replace cap after use.
OTC monograph final
RETAINE HPMC- HYPROMELLOSE 2910 (4000 MPA.S) SOLUTION/ DROPS OCUSOFT, 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._ ---------- DRUG FACTS ACTIVE INGREDIENT HYPROMELLOSE 0.3% PURPOSE EYE LUBRICANT USES ▪ FOR THE TEMPORARY RELEIF 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 ITTITATION. WARNINGS ▪ FOR USE IN THE EYES ONLY. DO NOT USE IF SOLUTION CHANGES COLOR OR BECOMES CLOUDY. WHEN USING THIS PRODUCT ▪ do not touch tip of container to any surface to avoid contamination. ▪ replace cap after use. STOP USE AND ASK A DOCTOR IF ▪ YOU EXPERIENCE EYE PAIN, CHANGES IN VISION, CONTINUED REDNESS OR IRRITATION OF THE EYE. ▪ 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 immediately. DIRECTIONS ▪ Instill 1 or 2 drops in the affected eye(s) as needed. OTHER INFORMATION ▪ Use only it tamper seals on top ad bottom flaps are intact. ▪ Store between 15°-30°C (59°-86°F). ▪ Keep carton for complete product information. ▪ Discard after 12 weeks. INACTIVE INGREDIENTS Citric acid, sodium citrate, sorbitol, water for injection. QUESTIONS? ☏(800)233-5469 M-F 8:30AM-5:00PM CST www.retainebrand.com PRINCIPAL DISPLAY PANEL OCuSOFT, Inc. RETAINE HPMC hypromellose 2910 (4000 mpa.s) solution/ drops PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:54799-896 ROUTE OF ADMINISTRATION OPHTHALMIC, TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) (Hypromellose 2910 (4000 Mpa.s) - UNII:RN3152OP35) Hypromellose 2910 (4000 Mpa.s) 3 mg in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SODIUM CITRATE (UNII: 1Q73Q2J קרא את המסמך השלם