WHISKCARE 357- benzalkonium chloride soap

WhiskCare 357 by

Drug Labeling and Warnings

WhiskCare 357 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 0.13%

Purpose

Antimicrobial

Uses

• For hand washing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness devleops, or if condition persists for more than 72 hours.

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

Directions

• Pump a small amount of foam into palm of hand.
• Rub thoroughly over all surfaces of both hands for fifteen seconds.
• Rinse with potable water.

Inactive Ingredients

Water, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WHISKCARE 357 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65585-509
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCO GLUCOSIDE (UNII: ICS790225B)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Characteristics
Color	white (water-white, dispensed as a white foam)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65585-509-01	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/29/2012	03/31/2022
2	NDC: 65585-509-02	208198 mL in 1 DRUM; Type 0: Not a Combination Product	10/29/2012	03/31/2022
3	NDC: 65585-509-03	8 in 1 BOX	10/29/2012	03/31/2022
3		1000 mL in 1 BAG; Type 0: Not a Combination Product
4	NDC: 65585-509-04	6 in 1 BOX	10/29/2012	03/31/2022
4		500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
5	NDC: 65585-509-05	6 in 1 BOX	10/29/2012	03/31/2022
5		1750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
6	NDC: 65585-509-06	4 in 1 BOX	10/29/2012	03/31/2022
6		4000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
7	NDC: 65585-509-07	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/29/2012	03/31/2022
8	NDC: 65585-509-08	3 in 1 BOX	10/29/2012	03/31/2022
8		1200 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	10/29/2012	03/31/2022

Labeler - Whisk Products, Inc. (834270639)

Establishment
Name	Address	ID/FEI	Business Operations
Whisk Products, Inc.		834270639	manufacture(65585-509)