Label: EYES ALIVE EYECON LUBRICATING- carboxymethylcellulose sodium, unspecified form liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 69183-205-01, 69183-205-02 - Packager: DIVISION 5 LABS, 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 19, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only.
When using this product
- to avoid contamination, do not touch tip to any surface
- replace cap after using
- Directions
- Other Information
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton
-
INGREDIENTS AND APPEARANCE
EYES ALIVE EYECON LUBRICATING
carboxymethylcellulose sodium, unspecified form liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69183-205 Route of Administration INTRAOCULAR Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength CALCIUM CHLORIDE (UNII: M4I0D6VV5M) HYDROCHLORIC ACID (UNII: QTT17582CB) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM CHLORIDE (UNII: 660YQ98I10) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM LACTATE (UNII: TU7HW0W0QT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69183-205-01 1 in 1 CARTON 01/07/2019 1 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 2 NDC:69183-205-02 2 in 1 CARTON 01/07/2019 2 10 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 01/07/2019 Labeler - DIVISION 5 LABS, INC. (968198288)