Label: REFRESH DIGITAL PF- carboxymethylcellulose sodium, glycerin and polysorbate 80 solution/ drops
- NDC Code(s): 0023-6954-05, 0023-6954-30
- Packager: Allergan, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 28, 2022
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- 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, do not use.
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For external use only.
- Directions
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
REFRESH DIGITAL PF
carboxymethylcellulose sodium, glycerin and polysorbate 80 solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-6954 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 GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 10 mg in 1 mL POLYSORBATE 80 (UNII: 6OZP39ZG8H) (POLYSORBATE 80 - UNII:6OZP39ZG8H) POLYSORBATE 80 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) CASTOR OIL (UNII: D5340Y2I9G) ERYTHRITOL (UNII: RA96B954X6) LEVOCARNITINE (UNII: 0G389FZZ9M) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0023-6954-30 30 in 1 CARTON 08/01/2020 1 0.4 mL in 1 VIAL, PLASTIC; Type 0: Not a Combination Product 2 NDC:0023-6954-05 1 in 1 CARTON 08/01/2020 2 .40 mL in 1 VIAL, PLASTIC; 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 08/01/2020 Labeler - Allergan, Inc. (144796497)