Label: CARBOXYMETHYLCELLULOSE SODIUM EYE LUBRICANT- carboxymethylcellulose sodium, unspecified solution/ drops
- NDC Code(s): 42494-448-05
- Packager: Cameron Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 7, 2024
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
- Use
-
Warnings
For use in the eyes only
- Retain outer carton for full product drug facts.
When using this product
- Avoid contamination, do not touch tip of container to any surface.
- Replace cap after use.
Stop use and ask a doctor if
- You experience eye pain, changes in vision, continued redness or irritationn of the eye.
- The condition worsens or persists for more than 72 hours.
- Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - 2 Bottle Carton
TWIN PACK
CAMERON
PHARMACEUTICALS™Compare to Refresh Tears® Lubricant
Eye Drops active ingredients† †NDC 42494-448-05
Lubricant
Eye DropsCARBOXYMETHYLCELLULOSE SODIUM 0.5%
EYE LUBRICANTMOISTURIZING
- Relieves burning, irritation
& discomfort due to dryness - For mild to moderate dry eye
- Sterile
2 Bottles
0.5 OZ (15 mL) Each
1.0 OZ (30 mL) TOTAL
- Relieves burning, irritation
-
INGREDIENTS AND APPEARANCE
CARBOXYMETHYLCELLULOSE SODIUM EYE LUBRICANT
carboxymethylcellulose sodium, unspecified solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42494-448 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength CALCIUM CHLORIDE (UNII: M4I0D6VV5M) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM CHLORIDE (UNII: 660YQ98I10) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM LACTATE (UNII: TU7HW0W0QT) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42494-448-05 2 in 1 CARTON 10/18/2024 1 15 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M018 10/18/2024 Labeler - Cameron Pharmaceuticals (078371442)