SCRUBS HAND SANITIZER WIPE- hand sanitizer wipe cloth

SCRUBS Hand Sanitizer Wipe by

Drug Labeling and Warnings

SCRUBS Hand Sanitizer Wipe by is a Otc medication manufactured, distributed, or labeled by ITW Pro Brands. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Purpose

For hand washing to decrease bacteria on skin.

Recommended for repeated use.

Warnings

do not get into eyes. If contact occurs rinse eyes thoroughly with water.

Flammable. Keep away from heat and flame.

FOR EXTERNAL USE ONLY

Ask your doctor

If irritation arises and persists for more than 72 hours.

Active Ingredient

Benzalkonium Chloride

Keep out of the reach of children

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

Inactive Ingredients

Water

Mineral oil

Isopropyl myristate

Ethanol

C11-15 Pareth-5

Dosage and Administration

Wet hands thoroughly with product and allow to dry without wiping.

Children under six years of age should be supervised when using this product.

Indications and Usage

To decrease bacteria on the skin.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Children under six years of age should be supervised when using this product

Package Label

INGREDIENTS AND APPEARANCE

SCRUBS HAND SANITIZER WIPE 
hand sanitizer wipe cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51239-1909
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.00097 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
C11-15 PARETH-5 (UNII: 9G5POA2F31)
WATER (UNII: 059QF0KO0R)
MINERAL OIL (UNII: T5L8T28FGP)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51239-1909-1	4.12 mL in 1 PACKAGE; Type 0: Not a Combination Product	10/01/2016	01/09/2018
2	NDC: 51239-1909-2	206 mL in 1 CONTAINER; Type 0: Not a Combination Product	10/01/2016	04/01/2019
3	NDC: 51239-1909-3	351 mL in 1 CONTAINER; Type 0: Not a Combination Product	10/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/01/2016

Labeler - ITW Pro Brands (067952994)

Establishment
Name	Address	ID/FEI	Business Operations
ITW Pro Brands		067952994	manufacture(51239-1909)