Label: CARBOXYMETHYLCELLULOSE SODIUM 1%- carboxymethylcellulose sodium liquid
- NDC Code(s): 0536-1398-81
- Packager: Rugby Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
• For use in eyes only.
• Using this product, to avoid contamination, do not touch tip of container to any surface.
• Do not reuse. Once opened, discard after use.
• Do not touch single-use container tip to the eye.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Do not use
If solution changes color or becomes cloudy.
IF TAMPER EVIDENT SEAL IS TORN, BROKEN OR MISSING
Save carton for complete drug facts.
*This product is not manufactured or distributed by Allergan, Inc., owner of the registered trademark Refresh® Celluvisc® Lubricant Eye Gel Drops.
Distributed by:
RUGBY LABORATORIES
Indianapolis, IN 46268
Questions or comments?
Call (800) 616-2471
Rev. 08/23
R-155
Re-order No. 371161
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
CARBOXYMETHYLCELLULOSE SODIUM 1%
carboxymethylcellulose sodium liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0536-1398 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 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength CALCIUM CHLORIDE (UNII: M4I0D6VV5M) HYDROCHLORIC ACID (UNII: QTT17582CB) MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM) 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:0536-1398-81 30 in 1 CARTON 10/01/2023 10/01/2023 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 Drug M018 10/01/2023 10/01/2023 Labeler - Rugby Laboratories (079246066)