Otc - Active Ingredient
polyhexamethylene biguanide
Drop Dream Eye 2
FDA Label NDC 52345-6001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by K&j.c Co., Ltd for the product Drop Dream Eye 2 (NDC 52345-6001). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
poloxamer407, borax, oric acid, sodium hyaluronate, water, etc
Otc - Purpose
cleanses, rinses, disinfects, stores, lubricates and removed protein buildup
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
always use fresh solution to disinfacts, to not reuse solution
Warnings
keep in room temperature
Dosage & Administration
opthalmic use only
Package Label.Principal Display Panel
Label (Label)
* Please review the disclaimer below.
