Label: REFRESH CLASSIC- polyvinyl alcohol, povidone solution/ drops
- NDC Code(s): 50090-2358-1
- Packager: A-S Medication Solutions
- This is a repackaged label.
- Source NDC Code(s): 0023-0506
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 14, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
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Warnings
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For external use only.
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To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.
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Do not touch unit-dose tip to eye.
- If solution changes color or becomes cloudy, do not use.
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For external use only.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- HOW SUPPLIED
- Polyvinyl Alcohol, Povidone
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INGREDIENTS AND APPEARANCE
REFRESH CLASSIC
polyvinyl alcohol, povidone solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50090-2358(NDC:0023-0506) Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYVINYL ALCOHOL (UNII: 532B59J990) (POLYVINYL ALCOHOL - UNII:532B59J990) POLYVINYL ALCOHOL 14 mg in 1 mL POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE 6 mg in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) sodium chloride (UNII: 451W47IQ8X) hydrochloric acid (UNII: QTT17582CB) sodium hydroxide (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50090-2358-1 30 in 1 CARTON 04/21/2016 1 .4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 09/12/1985 Labeler - A-S Medication Solutions (830016429) Establishment Name Address ID/FEI Business Operations A-S Medication Solutions 830016429 RELABEL(50090-2358)