Land: Vereinigte Staaten
Sprache: Englisch
Quelle: NLM (National Library of Medicine)
HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) (HYPROMELLOSE 2910 (4000 MPA.S) - UNII:RN3152OP35)
Aurolab
TOPICAL
OTC DRUG
- For use as a lubricant to prevent further irritation or to relieve dryness of the eye - If you are sensitive to any ingredient in this product - If solution changes color or becomes cloudy For use as a lubricant to prevent further irritaion or to relieve dryness of the eye
OTC monograph final
HYPROMELLOSE EYE DROPS 0.7%- HYPROMELLOSE EYE DROPS 0.7% FOR SOLUTION AUROLAB _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._ ---------- ACTIVE INGREDIENT Hypromellose 0.7% BP w/v DIRECTIONS FOR USE lnstill 1or 2 drops in the affected eye, as needed INACTIVE INGREDIENT 1. Benzalkonium Chloride 2. Borax 3. Boric acid 4. EDTA disodium salt 5. Potassium chloride 6. Purified water 7. Sodiumchloride TAMPER PROTECTION For your protection a tamper evident ring is attached to the bottlecap Upon opening, this will separate from the cap and can be discarded Use only if this ring is present and attached when the bottle is first opened USE For use as a lubricant to prevent further irritation or to relieve dryness of the eye QUESTIONS Call: 1-800-103-7321 Email: info@aurolab.com Web: www.aurolab.com KEEP OUT OF REACH OF CHILDREN If swallowed, get medical help or contact a poison control center right away ASK DOCTOR If you experience eye pain Change in vision Continued redness(or) irritation of the eye Condition worsens or persists for more than 72 hours DO NOT USE If you are sensitive to any ingredient in this product If solution changes color or becomes cloudy DOSAGE Instill 1 or 2 drops in the affected eyes as needed WARNINGS For External Use Only INDICATIONS AND USAGE For use as a lubricant to prevent further irritaion or to relieve dryness of the eye EYE LUBRICANT Eye Lubricant CARTON LABEL HYPROMELLOSE EYE DROPS 0.7% hypromellose eye drops 0.7% for solution PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:16030-101 ROUTE OF ADMINISTRATION 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) 7 mg in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH BORIC ACID (UNII: R57ZHV85D4) WAT Lesen Sie das vollständige Dokument