Active Ingredient
Hypromellose USP 2% w/v
Aurovisc Lubricant Hypromellose 2208 (15000 Mpa.s) Solution/drops
FDA Label NDC 16030-302
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 Aurovisc Lubricant Hypromellose 2208 (15000 Mpa.s) Solution/drops (NDC 16030-302). 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, inactive ingredient, use, questions, keep out of reach of children, stop use, do not use, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
- Acetic acid 1%
- Calcium chloride
- Citric acid 0.1465%
- Magnesium Chloride
- Sodium chloride
- Sodium acetate,
- Sodium Citrate
- Potassium chloride
- Purified water.
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
- Transient blurring of vision
- Ocular discomfort or irritation
- Matting or Stickness of eyelashes
- Photophobia
- Hypersensitivity or edema of the eyelids
Do Not Use
- If the solution becomes dark brown or any floating particles are observed.
- If you are sensitive to any ingredient in this product
Warnings
For External use only
Indiacations And Usage
Do not use if package is damaged
Discard after a single use
Do not freeze
Do not resterilize
Purpose
Lubricant
Dose
Instill 1 or 2 drops in the affected eyes as needed
Package Carton
Hpmc (Hpmc)
* Please review the disclaimer below.
