Label: COMPLIMENTS ADVANCED RELIEF EYE DROPS 15ML- dextran 70, povidone, polyethylene glycol 400, tetrahydrozoline hydrochloride solution/ drops
- NDC Code(s): 55651-989-15
- Packager: KC Pharmaceuticals, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated March 21, 2023
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
-
Warnings
For use in the eye only
Do not use
- if you use a monoamine oxidase inhibitor (MAOI)
- if solution changes colour or becomes cloudy.
Ask a doctor or pharmacist before use if you
- have narrow angle glaucoma
- are pregnant or breastfeeding.
When using this product
- pupils may become enlarged temporarily
- to avoid contamination, do not touch tip of the container to any surface
- replace cap after using
- overuse of this product may cause increased redness of the eye.
- Directions
- OTHER SAFETY INFORMATION
- Inactive ingredients
- Questions?
- Compliments Advanced Relief Eye Drops 15mL
-
INGREDIENTS AND APPEARANCE
COMPLIMENTS ADVANCED RELIEF EYE DROPS 15ML
dextran 70, povidone, polyethylene glycol 400, tetrahydrozoline hydrochloride solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55651-989 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 70 0.1 g in 100 mL POVIDONE (UNII: FZ989GH94E) (POVIDONE, UNSPECIFIED - UNII:FZ989GH94E) POVIDONE 1 g in 100 mL TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE 0.05 g in 100 mL POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL, UNSPECIFIED - UNII:3WJQ0SDW1A) POLYETHYLENE GLYCOL 400 1 g in 100 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SODIUM BORATE (UNII: 91MBZ8H3QO) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55651-989-15 1 in 1 BOX 05/14/2022 1 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 05/14/2022 Labeler - KC Pharmaceuticals, Inc. (174450460) Establishment Name Address ID/FEI Business Operations KC Pharmaceuticals, Inc 174450460 manufacture(55651-989) , pack(55651-989) , label(55651-989)