Label: GOOD SENSE LUBRICATING PLUS- carboxymethylcellulose sodium solution, gel forming / drops
- NDC Code(s): 0113-0323-65
- Packager: L. Perrigo 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 May 14, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each single-use container)
- Purpose
- Uses
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Warnings
For external use only
When using this product
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
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Package/Label Principal Display Panel
Sterile
Lubricating Plus
Lubricant Eye Drops
Carboxymethylcellulose Sodium 0.5%
Moisturizing Relief
Immediate, Soothing Relief for Dry Eyes
Preservative-Free
Actual Size
Compare to active ingredient of Refresh Plus® Lubricant Eye Drops
100% SATISFACTION GUARANTEED
30 Sterile Single-Use Containers
0.01 FL OZ (0.4 mL) Each
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INGREDIENTS AND APPEARANCE
GOOD SENSE LUBRICATING PLUS
carboxymethylcellulose sodium solution, gel forming / dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0113-0323 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength CALCIUM CHLORIDE (UNII: M4I0D6VV5M) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM CHLORIDE (UNII: 660YQ98I10) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM LACTATE (UNII: TU7HW0W0QT) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) HYDROCHLORIC ACID (UNII: QTT17582CB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0113-0323-65 6 in 1 CARTON 11/11/2013 1 5 in 1 POUCH 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 11/11/2013 Labeler - L. Perrigo Company (006013346)