Label: REFRESH OPTIVE ADVANCED- carboxymethylcellulose sodium, glycerin, and polysorbate 80 solution/ drops
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NDC Code(s):
0023-4307-02,
0023-4307-03,
0023-4307-10,
0023-4307-15, view more0023-4307-20
- Packager: Allergan, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 September 13, 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. Replace cap after using.
- If solution changes color, do not use.
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For external use only.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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INGREDIENTS AND APPEARANCE
REFRESH OPTIVE ADVANCED
carboxymethylcellulose sodium, glycerin, and polysorbate 80 solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-4307 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 chlorite (UNII: G538EBV4VF) hydrochloric acid (UNII: QTT17582CB) sodium hydroxide (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0023-4307-03 1 in 1 CARTON 11/30/2011 1 3 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 2 NDC:0023-4307-10 1 in 1 CARTON 11/30/2011 2 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 3 NDC:0023-4307-20 2 in 1 CARTON 11/30/2011 3 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 4 NDC:0023-4307-02 1 in 1 CARTON 11/30/2011 4 2 mL in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:0023-4307-15 1 in 1 CARTON 11/30/2011 5 15 mL in 1 BOTTLE; 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 11/30/2011 Labeler - Allergan, Inc. (144796497)