DYNA-HEX 2- chlorhexidine gluconate liquid 
Xttrium Laboratories, Inc.

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4-oz Dyna-Hex 2

Drug Facts

Active ingredient

Chlorhexidine Gluconate 2% Solution

Purpose

Antiseptic

Uses

Warnings

For external use only

Allergy alert:

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

if an allergic reaction occurs, stop use and seek medical help right awau

Do not use

When using this product

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

Healthcare personnel handwash:

Patient preoperative skin preparation:

Skin wound and general skin cleaning:

Other information

Inactive ingredients

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

Questions or comments?

call 1-800-587-3721

Monday through Friday 8:00 AM to 4:30 PM CST

NDA 0116-1021-04

DYNA-HEX 2 ®

(Chlorhexidine Gluconate 2% Solution)

Antiseptic

Contains: 2% Chlorhexidine Gluconate

FOR EXTERNAL USE ONLY

For single-use

Net Contents: 4 fl oz (118 mL)

Distributed By:
Xttrium Laboratories, Inc.
Mount Prospect, IL 60056
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Dyna Hex 2 4oz single panel

DYNA-HEX  2
chlorhexidine gluconate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0116-1021
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0116-1021-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA01942201/01/2014
Labeler - Xttrium Laboratories, Inc. (007470579)
Registrant - Xttrium Laboratories, Inc. (007470579)
Establishment
NameAddressID/FEIBusiness Operations
Xttrium Laboratories, Inc.007470579manufacture(0116-1021)

Revised: 12/2023
Document Id: 0cd05cb2-8939-df4d-e063-6294a90a43fd
Set id: 6e5f9616-ddf5-19c4-e053-2991aa0a372a
Version: 4
Effective Time: 20231218
 
Xttrium Laboratories, Inc.