SKIP THE GERMS ANTIBACTERIAL HAND WASH- benzalkonium chloride soap

Skip The Germs Antibacterial Hand Wash by

Drug Labeling and Warnings

Skip The Germs Antibacterial Hand Wash by is a Otc medication manufactured, distributed, or labeled by Total Body Care Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride  0.13%

Purpose

Antimicrobial

Use

Kills harmful bacteria and moistens hands

Warnings

Warnings:

 For external use only

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

 Stop use and ask a doctor if irritation develops  Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away

 Do not use if you are allergic to any of these ingredients

DOSAGE & ADMINISTRATION

Inactive ingredients

Aqua/Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Decyl Glucoside, Glyceryn, Citric acid, Tetrasodium EDTA, Methylchloroisothiazolinone and Methylisothiazolinone, CI 19140, CI 42090, Parfum

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children 

Product Label 

INGREDIENTS AND APPEARANCE

SKIP THE GERMS ANTIBACTERIAL HAND WASH 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54369-002
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)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54369-002-01	200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/20/2020
2	NDC: 54369-002-02	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/20/2020
3	NDC: 54369-002-03	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/20/2020

Labeler - Total Body Care Inc (250919615)

Establishment
Name	Address	ID/FEI	Business Operations
Total Body Care Inc		250919615	manufacture(54369-002)