Drug Facts
Active Ingredient: PurposePovidone Iodine USP, 10% w/v Antiseptic(equivalent to 1% titratable Iodine)
Grx Dyne
FDA Label NDC 54162-269
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Geritrex Corp. for the product Grx Dyne (NDC 54162-269). 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 drug facts, uses, directions, dosage & administration, warnings, inactive ingredient, storage and handling, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
First aid antiseptic to help the risk of infection in minor cuts, scrapes or burns
Directions
Clean the affected area
Apply a small amount of this product to the area 1-3 times daily
May be covered with a sterile bandaged
If bandaged, let dry first
Dosage & Administration
Apply a small amount of this product to the affected area 1-3 times daily
Warnings
FOR EXTERNAL USE ONLYDO NOTUse in the eyesUse on individuals who are allergic of sensitive to iodineApply over large areas of the bodyDiscontinue use and ask a doctorIf condition persist or gets worseFor use longer than 1 weekAsk a doctor in case ofDeep or punctured woundsAnimal bitesSerious burns
Inactive Ingredient
Citric acid, glycerin, Nonoxynol 10, purified water, sodium hydroxide
Storage And Handling
Store at room temperature: 15'-30'C (59'-86'F)
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.
Package Label.Principal Display Panel
Label Of Bottle (Gpis4)
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