ANTISEPTIC SKIN CLEANSER- 2% chlorhexidine gluconate solution solution 
AmerisourceBergen Drug Corporation

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2% Good Neighbor Pharmacy

Active ingredient

Chlorhexidine gluconate 2% solution

Purpose

Antiseptic

Uses

Warnings

For external use only

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

If an allergic reaction occurs, stop use and seek medical help right away.

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

Surgical hand scrub:

Healthcare personnel handwash:

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

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.

GOOD NEIGHBOR PHARMACY®

NDC 46122-659-36

Advanced Antibacterial Hand Soap

CHLORHEXIDINE GLUCONATE 2% SOLUTION

ANTISEPTIC/ANTIMICROBIAL SKIN CLEANSER

8.5 FL OZ (250 mL)

2GNP85FBTLLBL

2GNP85 PDP

2GNP85 DF1

2GNP85 DF2

2GNP85 DF3

ANTISEPTIC SKIN CLEANSER 
2% chlorhexidine gluconate solution solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-659
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE2 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
WATER (UNII: 059QF0KO0R)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-659-36250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA01942210/01/2020
Labeler - AmerisourceBergen Drug Corporation (007914906)
Registrant - Xttrium Laboratories, Inc. (007470579)
Establishment
NameAddressID/FEIBusiness Operations
Xttrium Laboratories, Inc.007470579manufacture(46122-659)

Revised: 10/2020
Document Id: b1030a94-28eb-36bf-e053-2a95a90a315a
Set id: b1030a94-28ea-36bf-e053-2a95a90a315a
Version: 1
Effective Time: 20201006
 
AmerisourceBergen Drug Corporation