Label: CVS LUBRICANT EYE DROPS 30 CT- carboxymethylcellulose soduim liquid
- NDC Code(s): 69842-993-01
- Packager: CVS Pharmacy, 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 July 15, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only
When using this product
- do not reuse
- once opened, discard
- to avoid contamination, do not touch tip of container to any surface
- do not touch unit-dose tip to eye
- Directions
- Other information
- Inactive ingredients
- CVS Lubricant Eye Drops 30 ct
-
INGREDIENTS AND APPEARANCE
CVS LUBRICANT EYE DROPS 30 CT
carboxymethylcellulose soduim liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-993 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 MAGNESIUM CHLORIDE (UNII: 02F3473H9O) WATER (UNII: 059QF0KO0R) SODIUM LACTATE (UNII: TU7HW0W0QT) SODIUM CHLORIDE (UNII: 451W47IQ8X) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) POTASSIUM CHLORIDE (UNII: 660YQ98I10) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-993-01 30 in 1 BOX 07/15/2019 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 07/15/2019 Labeler - CVS Pharmacy, Inc. (062312574) Registrant - KC Pharmaceuticals, Inc. (174450460) Establishment Name Address ID/FEI Business Operations Unimed 689852052 manufacture(69842-993) , pack(69842-993) , label(69842-993)