SCRUBS LEMON HAND SANITIZER WIPES- hand sanitizer wipes cloth
ITW Pro Brands

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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LEMON Hand Sanitizer Wipes

Active Ingredients

Purpose

Uses

For hand washing to decrease bacteria on skin.

Recommended for repeated use.

Warnings

When using this product

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

Flamable. Keep away from heat and flalme.

FOR EXTERNAL USE ONLY

Stop Use

Stop use and ask a doctor

If irritation arises and persists for more than 72 hours.

Keep Out of the Reach of Children

Stop use and ask a doctor

If irritation arises and persists for more than 72 hours.

Inactive Ingredients

water

mineral oil

isopropyl myristate

alcohol

Watch highlighted

•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

•For hand washing to decrease bacteria on skin.

•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 Principal Display Panel

SCRUBS Lemon Wipes

SCRUBS LEMON HAND SANITIZER WIPES
hand sanitizer wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:51239-0929
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g in 970 mL
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.1 g in 970 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)	20 g in 970 mL
WATER (UNII: 059QF0KO0R)	78.1 g in 970 mL
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	0.3 g in 970 mL
MINERAL OIL (UNII: T5L8T28FGP)	0.7 g in 970 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:51239-0929-0	4 mL in 1 PACKET; Type 0: Not a Combination Product	11/01/2009	10/01/2016
2	NDC:51239-0929-1	438 mL in 1 CONTAINER; Type 0: Not a Combination Product	11/01/2009	10/01/2016
3	NDC:51239-0929-2	77 mL in 1 PACKAGE; Type 0: Not a Combination Product	11/01/2009	10/01/2016
4	NDC:51239-0929-3	206 mL in 1 CONTAINER; Type 0: Not a Combination Product	11/01/2009	10/01/2016
5	NDC:51239-0929-4	619 mL in 1 CONTAINER; Type 0: Not a Combination Product	11/01/2009	10/01/2016
6	NDC:51239-0929-5	1134 mL in 1 CONTAINER; Type 0: Not a Combination Product	11/01/2009	10/01/2016
7	NDC:51239-0929-6	1247 mL in 1 CONTAINER; Type 0: Not a Combination Product	11/01/2009	10/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333	10/01/2009	10/01/2016

Labeler - ITW Pro Brands (067952994)

Name	Address	ID/FEI	Business Operations
Establishment
ITW Pro Brands		067952994	manufacture(51239-0929)

Revised: 1/2018

Document Id: 635fe378-13b0-1cec-e053-2991aa0a15a1

Set id: be03f82f-087d-4d63-a7f7-aaa64c4735d9

Version: 5

Effective Time: 20180122

ITW Pro Brands