GERM FREE TOPICAL ANTISEPTIC- benzalkonium chloride gel

Germ Free Topical Antiseptic by

Drug Labeling and Warnings

Germ Free Topical Antiseptic 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:

First aid antiseptic - Topical skin treatment

Uses:

First aid soothing and germ protection for:

Minor cuts  Scrapes  Burns  Skin irritations  Minor abrasions

Warnings:

• Do not freeze, For external use only.

Do not use

In ears, eyes or mouth.

When using this product,

• avoid contact with the eyes. In case of contact, flush eyes with water.

Stop use and ask doctor if

redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children.

• Children should be supervised when using this product.

Directions:

• Apply liberally over effected area, recommended for repeat application regularly.

Inactive Ingredinets:

1-Octadecyldimethyl (3-Trimethoxysilylpropyl) ammonium chloride, Aloe Barbadenis leaf extract, Aqua, Caprylyl Glucoside, Citric Acid, Hydroxyethyl cellulose, Polyhexanide, Phenoxyethanol.

Questions?

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

Package Labeling:

INGREDIENTS AND APPEARANCE

GERM FREE TOPICAL ANTISEPTIC 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-008
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)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POLIHEXANIDE (UNII: 322U039GMF)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-008-02	57 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	part333A	12/01/2018

Labeler - ESC Brands, LLC (202621850)