GRX DYNE- povidone iodine solution

GRx Dyne by

Drug Labeling and Warnings

GRx Dyne by is a Otc medication manufactured, distributed, or labeled by Geritrex Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient:                      Purpose

Povidone Iodine USP, 10% w/v  Antiseptic

(equivalent to 1% titratable Iodine)

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 ONLY

DO NOT

Use in the eyes

Use on individuals who are allergic of sensitive to iodine

Apply over large areas of the body

Discontinue use and ask a doctor

If condition persist or gets worse

For use longer than 1 week

Ask a doctor in case of

Deep or punctured wounds

Animal bites

Serious 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)

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.

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

GRX DYNE 
povidone iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54162-269
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (POVIDONE-IODINE - UNII:85H0HZU99M)	POVIDONE-IODINE	10 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
NONOXYNOL-10 (UNII: K7O76887AP)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54162-269-16	472 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/16/2012

Labeler - Geritrex Corp. (112796248)