Label: WALGREENS LUBRICANT EYE DROPS HIGH PERFORMANCE 15ML AND TWIN PACK- polyethylene glycol 400, propylene glycol liquid
- NDC Code(s): 0363-4549-01, 0363-4549-02
- Packager: Walgreen Company
- 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 October 17, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
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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
- Questions or comments?
- Walgreens Lubricant Eye Drops High Performance 15mL
- Walgreens Lubricant Eye Drops High Performance 15mL twin pack
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INGREDIENTS AND APPEARANCE
WALGREENS LUBRICANT EYE DROPS HIGH PERFORMANCE 15ML AND TWIN PACK
polyethylene glycol 400, propylene glycol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-4549 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 0.3 g in 100 mL POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL, UNSPECIFIED - UNII:3WJQ0SDW1A) POLYETHYLENE GLYCOL 400 0.4 g in 100 mL Inactive Ingredients Ingredient Name Strength AMINOMETHYLPROPANOL (UNII: LU49E6626Q) BORIC ACID (UNII: R57ZHV85D4) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SORBITOL (UNII: 506T60A25R) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) POTASSIUM CHLORIDE (UNII: 660YQ98I10) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-4549-01 1 in 1 BOX 10/15/2019 1 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 2 NDC:0363-4549-02 2 in 1 BOX 10/15/2019 2 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 final part349 10/15/2019 Labeler - Walgreen Company (008965063) Registrant - KC Pharmaceuticals, Inc. (174450460) Establishment Name Address ID/FEI Business Operations KC Pharmaceuticals, Inc. 174450460 pack(0363-4549) , label(0363-4549) , manufacture(0363-4549)