GRX DYNE SCRUB- povidone-iodine solution

GRx Dyne Scrub by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Active Ingredient:                      Purpose

Povidone-Iodine, 7.5%              Antiseptic

(Equal to 0.75% available Iodine)

uses

Disinfectant hand wash and skin cleanser.

Significantly reduces bacteria on the skin.

Directions

Wet skin and apply a sufficient amount for lather to

cover all surfaces.

Wash vigorously for at least 15 seconds.

Rinse and dry thoroughly.

DOSAGE & ADMINISTRATION

Wash vigorously for at least 15 seconds.

Warnings

For External Use Only

Do not use this product:

If you are sensitive to iodine or other products ingredients.

In the eyes.

Over large areas of the body.

Longer than 1 week unless directed by a doctor.

Ask a doctor before use if you have

Deep puncture wounds: serious burns: or animal bites.

Stop using this product and ask a doctor if;

Redness, irritation, swelling, or pain continues or increases, or infection occurs.

Inactive Ingredient

Citric acid, glycerin, Nonoxynol 10, purified water, sodium hydroxide

STORAGE AND HANDLING

Store at 25'C (77'F); excursions permitted between

15'-30'C (59'-86'F)

KEEP OUT OF REACH OF CHILDREN

If swallowed get medical help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

Enter section text here

INGREDIENTS AND APPEARANCE

GRX DYNE SCRUB 
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54162-268
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (POVIDONE-IODINE - UNII:85H0HZU99M)	POVIDONE-IODINE	7500 mg  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: 54162-268-04	118 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	07/03/2012

Labeler - Geritrex Corp. (112796248)