Label: QUALITY CHOICE LUBRICANT EYE DROPS LONG LASTING- polyethylene glycol 400, propylene glycol solution/ drops
- NDC Code(s): 83324-030-15
- Packager: Chain Drug Marketing Assoc., Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 19, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purposes
- Use
-
Warnings
For external use only
Do not use
- if this product changes color or becomes cloudy
- if you are sensitive to any ingredient in this product
When using this product
- do not touch tip of container to any surface to avoid contamination
- replace cap after each use
- Directions
- Other information
- Inactive ingredients
- Quality Choice Lubricant Eye Drops Long Lasting 15mL
-
INGREDIENTS AND APPEARANCE
QUALITY CHOICE LUBRICANT EYE DROPS LONG LASTING
polyethylene glycol 400, propylene glycol solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-030 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 400 0.4 g in 100 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 0.3 g in 100 mL Inactive Ingredients Ingredient Name Strength POTASSIUM CHLORIDE (UNII: 660YQ98I10) SODIUM BORATE (UNII: 91MBZ8H3QO) BORIC ACID (UNII: R57ZHV85D4) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) ZINC CHLORIDE (UNII: 86Q357L16B) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83324-030-15 1 in 1 BOX 12/19/2023 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 OTC Monograph Drug M018 12/19/2023 Labeler - Chain Drug Marketing Assoc., Inc. (011920774) Registrant - KC Pharmaceuticals, Inc. (174450460) Establishment Name Address ID/FEI Business Operations KC Pharmaceuticals, Inc. 174450460 pack(83324-030) , manufacture(83324-030) , label(83324-030)