Label: MEIJER LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops
- NDC Code(s): 79481-0066-1, 79481-0066-2
- Packager: Meijer Distribution, 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 November 8, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- 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
- Questions or comments?
- Meijer Lubricant Eye Drops 30ct
- Meijer Lubricant Eye Drops 70ct
-
INGREDIENTS AND APPEARANCE
MEIJER LUBRICANT EYE DROPS
carboxymethylcellulose sodium solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-0066 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 SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM HYDROXIDE (UNII: 55X04QC32I) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) HYDROCHLORIC ACID (UNII: QTT17582CB) WATER (UNII: 059QF0KO0R) SODIUM LACTATE (UNII: TU7HW0W0QT) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM CHLORIDE (UNII: 660YQ98I10) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79481-0066-1 30 in 1 BOX 11/08/2020 1 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product 2 NDC:79481-0066-2 70 in 1 BOX 11/08/2020 2 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 11/08/2020 Labeler - Meijer Distribution, Inc. (006959555) Registrant - KC Pharmaceuticals, Inc. (174450460) Establishment Name Address ID/FEI Business Operations KC Pharmaceuticals, Inc. 174450460 pack(79481-0066) , label(79481-0066) Establishment Name Address ID/FEI Business Operations Unimed 689852052 manufacture(79481-0066)