Label: REFRESH RELIEVA PF- carboxymethylcellulose sodium and glycerin solution/ drops
- NDC Code(s): 0023-4515-30, 0023-9537-05
- Packager: Allergan, Inc.
- Category: HUMAN OTC DRUG LABEL
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 Label Information
Updated June 24, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
-
Warnings
-
For external use only.
-
To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.
-
Do not touch unit-dose tip to eye.
- If solution changes color, do not use.
-
For external use only.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
REFRESH RELIEVA PF
carboxymethylcellulose sodium and glycerin solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-4515 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 Inactive Ingredients Ingredient Name Strength CALCIUM CHLORIDE (UNII: M4I0D6VV5M) ERYTHRITOL (UNII: RA96B954X6) LEVOCARNITINE (UNII: 0G389FZZ9M) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM CHLORIDE (UNII: 660YQ98I10) WATER (UNII: 059QF0KO0R) SODIUM LACTATE (UNII: TU7HW0W0QT) HYALURONATE SODIUM (UNII: YSE9PPT4TH) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0023-4515-30 30 in 1 CARTON 09/25/2020 1 0.4 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 final part349 09/25/2020 REFRESH RELIEVA PF
carboxymethylcellulose sodium and glycerin solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-9537 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 Inactive Ingredients Ingredient Name Strength CALCIUM CHLORIDE (UNII: M4I0D6VV5M) ERYTHRITOL (UNII: RA96B954X6) LEVOCARNITINE (UNII: 0G389FZZ9M) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM CHLORIDE (UNII: 660YQ98I10) WATER (UNII: 059QF0KO0R) SODIUM LACTATE (UNII: TU7HW0W0QT) HYALURONATE SODIUM (UNII: YSE9PPT4TH) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0023-9537-05 5 in 1 CARTON 09/25/2020 1 0.4 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 final part349 09/25/2020 Labeler - Allergan, Inc. (144796497)