WHISKCARE 355- benzalkonium chloride soap

WhiskCare 355 by

Drug Labeling and Warnings

WhiskCare 355 by is a Otc medication manufactured, distributed, or labeled by Whisk Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WHISKCARE 355 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65585-555
Route of Administration	Topical

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	25 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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
Color	yellow (very pale yellow - very pale gold)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65585-555-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/20/2007	06/30/2021
2	NDC: 65585-555-02	236.6 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/20/2007	06/30/2021
3	NDC: 65585-555-03	59 mL in 1 TUBE; Type 0: Not a Combination Product	09/20/2007	06/30/2021
4	NDC: 65585-555-04	12 in 1 BOX	09/20/2007	01/03/2017
4		800 mL in 1 BAG; Type 0: Not a Combination Product
5	NDC: 65585-555-05	208198 mL in 1 DRUM; Type 0: Not a Combination Product	09/20/2007	06/30/2021
6	NDC: 65585-555-06	6 in 1 BOX	09/20/2007	06/30/2021
6		1750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7	NDC: 65585-555-07	4 in 1 BOX	09/20/2007	06/30/2021
7		4000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
8	NDC: 65585-555-08	8 in 1 BOX	09/20/2007	06/30/2021
8		1000 mL in 1 BAG; Type 0: Not a Combination Product
9	NDC: 65585-555-09	12 in 1 BOX	05/14/2019	06/30/2021
9		800 mL in 1 BAG; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/20/2007	06/30/2021

Labeler - Whisk Products, Inc. (834270639)

Establishment
Name	Address	ID/FEI	Business Operations
Whisk Products, Inc.		834270639	manufacture(65585-555)