ISO-SHIELD HAND SANITIZER- benzalkonium chloride liquid

ISO-SHIELD Hand Sanitizer by

Drug Labeling and Warnings

ISO-SHIELD Hand Sanitizer 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 & Skin Sanitizer

Uses:

Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use

Warnings:

Do not freeze, For external use only.

Do nout 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 a doctor

• if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

• Children should be supervised when using this product.

Directions

Apply lberally to the palms of the hands.  Rub into skin until dry.  Recocmmended for repeated use.

Inactive Ingredients:

1-octadecyldimethyl (3-triethoxysilylpropyl), Ammonium Chloride, Aloe Barbadenis Leaf Extract, Aqua, C12-C15 Pareth 12, Caprylyl Glucoside, Polyhexanide, Phenoxyethanol, Triethanolamine

Questions?

+1 (800) 797-1405 Mon-Fri 9:00am-5.00PM (PST)

Package Labeling:

INGREDIENTS AND APPEARANCE

ISO-SHIELD HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-005
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
AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
C12-15 PARETH-12 (UNII: 131316X18L)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
POLIHEXANIDE (UNII: 322U039GMF)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-005-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/14/2018

Labeler - ESC BRANDS LLC (202621850)