Active Ingredient
Carboxymethylcellulose sodium IP 0.5% w/v
Auro-cmc For Solution
FDA Label NDC 16030-401
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aurolab for the product Auro-cmc (NDC 16030-401). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, directions for use, inactive ingredient, use, questions, keep out of reach of children, stop use and ask a doctor if, do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Directions For Use
- lnstill 1or 2 drops in the affected eye, as needed
Inactive Ingredient
- Boric acid
- Calcium chloride
- Magnesium chloride
- Potassium chloride
- Water
- Sodium tetra borate
Use
For use as a lubricant to prevent further irritation or to relieve dryness of the eye
Questions
Call. 1-800-103-7321
E-mail : [email protected]
Web : www.aurolab.com
Keep Out Of Reach Of Children
If swallowed get medical help or contact a Poison Control Center right away
Stop Use And Ask A Doctor If
1.You experience eye pain
2.Change in vision Continued redness (or) irritation of the eye
Do Not Use
1.If you are sensitive to any ingredient in this product
2.If solution changes color or becomes cloudy
Warnings
For external use only
Indication & Usage
Do not touch the nozzle tip to any surface since this may contaminate the solution
Replace cap after using
Dose
Instill 1 or 2 drops in the affected eyes as needed
Eye Lubricant
Eye lubricant
Package Carton
Aurocmc (Aurocmc)
* Please review the disclaimer below.
