WHISKCARE 355- benzalkonium chloride soap 
Whisk Products, 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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​Active Ingredient

Benzalkonium Chloride 2.5%

​Purpose

Skin Sanitizer

​Use

reduces amount of bacteria on hands

​Warnings

Avoid contact with eyes.  If contents come in contact with eyes, flush eyes with water for at least 15 minutes & get medical attention.

For external use only.

If irritation develops, use of this product should be discontinued.  If irritation persists for more than 72 hours, consult a physician.

Do not allow concentrate to come in contact with food.

For institutional and professional use only.

​Directions

  • Hands need not be washed prior to using.
  • Dispense a small amount into palm of hand.
  • Wash for at least 15 seconds.
  • Rinse with potable water.
  • Repeat as needed.

​Inactive Ingredients

Water, Cocamidopropyl Betaine, Cocamidopropylamine Oxide, PEG-6 Cocamide, Hydroxypropyl Methylcellulose, Quaternium-15, Citric Acid, Sodium Hydroxide

8 x 1000 mL CleanShot Bags

WHISKCARE 355 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65585-555
Route of AdministrationTopical
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
QUATERNIUM-15 (UNII: E40U03LEM0)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Product Characteristics
Coloryellow (very pale yellow - very pale gold) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65585-555-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product09/20/200706/30/2021
2NDC:65585-555-02236.6 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/20/200706/30/2021
3NDC:65585-555-0359 mL in 1 TUBE; Type 0: Not a Combination Product09/20/200706/30/2021
4NDC:65585-555-0412 in 1 BOX09/20/200701/03/2017
4800 mL in 1 BAG; Type 0: Not a Combination Product
5NDC:65585-555-05208198 mL in 1 DRUM; Type 0: Not a Combination Product09/20/200706/30/2021
6NDC:65585-555-066 in 1 BOX09/20/200706/30/2021
61750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7NDC:65585-555-074 in 1 BOX09/20/200706/30/2021
74000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
8NDC:65585-555-088 in 1 BOX09/20/200706/30/2021
81000 mL in 1 BAG; Type 0: Not a Combination Product
9NDC:65585-555-0912 in 1 BOX05/14/201906/30/2021
9800 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/20/200706/30/2021
Labeler - Whisk Products, Inc. (834270639)
Establishment
NameAddressID/FEIBusiness Operations
Whisk Products, Inc.834270639manufacture(65585-555)

Revised: 3/2020
Document Id: e53bb999-b5df-4120-860c-9510bd06aeb8
Set id: 33979dd0-8718-46bd-8466-6c9aed31d330
Version: 4
Effective Time: 20200306
 
Whisk Products, Inc.