DYNA-HEX 2- chlorhexidine gluconate 2% solution

Dyna-Hex 2 by

Drug Labeling and Warnings

Dyna-Hex 2 by is a Otc medication manufactured, distributed, or labeled by Xttrium Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Chlorhexidine gluconate 2% solution

Purpose

Antiseptic

Uses

• surgical hand scrub: significantly reduces the number of microorganisms on the hands and forearms prior to surgery or patient care
• healthcare personnel handwash: helps reduce bacteria that potentially can cause disease

WARNINGS

For external use only

Allergy alert:
This product may cause a severe allergic reaction. Symptoms may include:

 wheezing/difficulty breathing
 shock
 facial swelling
 hives
 rash
If an allergic reaction occurs, stop use and seek medical help right away.

Do not use

• if you or the patient are allergic to chlorhexidine gluconate or any other ingredient in this product

When using this product

 keep out of eyes, ears, and mouth. May cause serious and permanent eye injury if permitted to enter and remain in the eye or may cause deafness when instilled in the middle ear through perforated eardrums.
 if solution should contact these areas, rinse out promptly and thoroughly with water
 wounds which involve more than the superficial layers of the skin should not be routinely treated

Stop use and ask a doctor if

irritation, sensitization, or allergic reaction occurs. These may be signs of a serious condition.

Keep out of reach of children

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

Directions

use with care in premature infants or infants under 2 months of age. These products may cause irritation or chemical burns.
Surgical hand scrub:
 wet hands and forearms with water
 scrub for 3 minutes with 5 mL of solution (4 full strokes) and a wet brush, paying close attention to the nails, cuticles and interdigital spaces
 a separate nail cleaner may be used
 rinse thoroughly
 wash for an additional 3 minutes with 5 mL of solution (4 full strokes) and rinse under running water
 dry thoroughly
Healthcare personnel handwash:
 wet hands with water
 dispense 5 mL of solution (4 full strokes) into cupped hands and wash in a vigorous manner for 15 seconds
 rinse and dry thoroughly

Other information

 store at 20-25°C (68-77°F)
 avoid excessive heat above 40°C (104°F)

INACTIVE INGREDIENT

citric acid, cocamide DEA, hydroxyethylcellulose, isopropyl alcohol, lauramine oxide, purified water

Questions or comments?

Questions or comments?
call 1-800-587-3721 Monday through Friday 8:00 AM to 4:30 PM CST

Laundering/Cleaning Instructions:

Chlorhexidine gluconate skin cleansers will cause stains if used with chlorine releasing products, such as chlorine bleach. Rinse completely and use only non-chlorine detergents.

PRINCIPAL DISPLAY PANEL

NDC: 0116-1022-32

DYNA-HEX 2®

Chlorhexidine Gluconate 2% Solution Antiseptic

Contains: 2% Chlorhexidine Gluconate

Distributed By: Xttrium Laboratories, Inc. Mount Prospect, IL 60056

CHLORHEXIDINE GLUCONATE
Net Contents: 32 fl oz (1 qt) (946 mL)

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INGREDIENTS AND APPEARANCE

DYNA-HEX 2 
chlorhexidine gluconate 2% solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0116-1022
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0116-1022-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/14/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA019422	12/14/2023

Labeler - Xttrium Laboratories, Inc. (007470579)

Registrant - Xttrium Laboratories, Inc. (007470579)

Establishment
Name	Address	ID/FEI	Business Operations
Xttrium Laboratories, Inc.		007470579	manufacture(0116-1022)