KLAR AND DANVER ANTIBACTERIAL HAND- benzalkonium chloride soap 
Greenbrier International, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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KLAR & DANVER ANTIBACTERIAL LIQUID HAND SOAP

KLAR & DANVER ANTIBACTERIAL LIQUID HAND SOAP


Active Ingredient

Benzalkonium Chloride 0.10%

Purpose

Antibacterial

Use:

Handwashing to decrease bacteria on skin.

Warnings:

For external use only.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develop or increase.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

  • Wet hands, work into a rich lather
  • Rinse well.

Inactive Ingredients:

WATER, SODIUM LAURYL ETHER SULFATE, COCAMIDOPROPYL BETAINE, SODIUM CHLORIDE, POLYQUATERNIUM-7, FRAGRANCE, METHYLISOTHIAZOLINONE, METHYLCHLOROISOTHIASOLINONE, CITRIC ACID, GLUTARIC DIALDEHYDE, TETRASODIUM EDTA, TOCOPHERYL ACETATE (VITAMIN E), ALOE BARBADENSIS LEAF EXTRACT, FD C ORANGE 7 (CI 15510).

DISTRIBUTED BY

GREENBRIER INTERNATIONAL, INC.

500 VOLVO PARKWAY, CHESAPEAKE, VA 23320

MADE IN  MEXICO

KLAR and DANVER ANTIBACTERIAL LIQUID HAND SOAP 1,584 Bottles (443ml each) (33992-8000-0)

Label


KLAR and DANVER ANTIBACTERIAL LIQUID HAND SOAP 1,210 Bottles (591ml each) (33992-8000-1)

Label20oz







KLAR AND DANVER ANTIBACTERIAL HAND 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:33992-8000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:33992-8000-01584 in 1 CONTAINER08/28/201307/07/2020
1443 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:33992-8000-11210 in 1 CONTAINER08/28/201307/07/2020
2591 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/28/201307/07/2020
Labeler - Greenbrier International, Inc. (610322518)
Registrant - 4E Global, S.A.P.I. de C.V. (812821307)
Establishment
NameAddressID/FEIBusiness Operations
4E Global, S.A.P.I. de C.V.812821307manufacture(33992-8000)

Revised: 12/2021
 
Greenbrier International, Inc.