GERM FREE SANITIZING- benzalkonium chloride soap

Germ Free Sanitizing by

Drug Labeling and Warnings

Germ Free Sanitizing by is a Otc medication manufactured, distributed, or labeled by ESC Brands, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose:

Antiseptic Hand Soap

Uses:

• Handwash to help reduce bacteria that potentially can cause disease
• Helps to prevent cross- contamination by hand contact
• Helps to prevent drying of skin
• Recommended for repeat use

Warnings:

• For external use only

When using this product

do not use in or near eyes

Stop use and ask doctor if

irritation and redness develop

Keep out of reach of children.

If swallowed. seek medical attention or contact a Posion Control Center immediately.

Directions:

• Wet Hands and wrists with clean running water
• Apply appropriate amount of product
• Lather and scrub hands, fingers, fingernails, cuticles and wrists thoroughly
• Rinse thoroughly with running water
• Dry hands completely (incomplete drying may result in chapped skin)

Other Information

Store in a cool dry place below 104° F (40°C)

Inactive Ingredinets:

Aloe Barbadensis Leaf Juice, Aqua, Benzyl Alcohol, Citric Acid, Glycerin, Hydrolysed Silk, Lauramidopropyl Betaine, Phenoxyethanol.

Questions?

+1(888) 331-8332, Mon-Fri 9:00AM-5:00PM (EST)

Package Labeling:

INGREDIENTS AND APPEARANCE

GERM FREE SANITIZING 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-007
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-007-08	245 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/01/2018

Labeler - ESC Brands, LLC (202621850)