TOPCARE ANTIBACTERIAL WHITE TEA FOAMING HAND- benzalkonium chloride soap 
Abaco Partners LLC DBA Surefil

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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TopCare ® Antibacterial White Tea Foaming Hand Soap

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

for handwashing, reduces germs on the skin

Warnings

For external use only–hands only

When using this product

  • Avoid contact with eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

  • irritation and redness develops.

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

Directions

Inactive ingredients

Purified Water, Lauramine Oxide, Glycerin, Cocamidopropyl Betaine, Isostearamidopropyl Ethyldimonium Ethosulfate, Fragrance, DMDM Hydantoin, Tetrasodium EDTA, Hydroxypropyl Methyl Cellulose, Chlorhexidine Gluconate, Zinc Sulfate Monohydrate, Citric Acid, FD&C Red #33 (CI17200), FD&C Blue #1 (CI42090)

Other information

store at 20°C - 25°C (68°F - 77°F)

Questions?

Call 1-888-423-0139

DISTRIBUTED BY TOPCO ASSOCIATES LLC
ELK GROVE VILLAGE, IL 60007

PRINCIPAL DISPLAY PANEL - 221 mL Bottle Label

TopCare ®

ANTIBACTERIAL
foaming
hand soap

gentle enough
for every day

WHITE TEA

7.5 FL OZ (221 mL)

PRINCIPAL DISPLAY PANEL - 221 mL Bottle Label
TOPCARE ANTIBACTERIAL WHITE TEA FOAMING HAND 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20890-0120
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
GLYCERIN (UNII: PDC6A3C0OX)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
ISOSTEARAMIDOPROPYL ETHYLDIMONIUM ETHOSULFATE (UNII: U059JNZ17L)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
EDETATE SODIUM (UNII: MP1J8420LU)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
ZINC SULFATE MONOHYDRATE (UNII: PTX099XSF1)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:20890-0120-1221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/01/2016
Labeler - Abaco Partners LLC DBA Surefil (964809417)
Establishment
NameAddressID/FEIBusiness Operations
Abaco Partners LLC DBA Surefil964809417manufacture(20890-0120)

Revised: 12/2021
Document Id: d428c681-4b40-4d8e-e053-2a95a90a8611
Set id: 1a4df61a-0a6e-4427-b3dc-48f52d1e5bfe
Version: 2
Effective Time: 20211227
 
Abaco Partners LLC DBA Surefil