MY-SHIELD SANITIZING HAND WIPES- benzalkonium chloride swab

My-Shield Sanitizing Hand Wipes by

Drug Labeling and Warnings

My-Shield Sanitizing Hand Wipes by is a Otc medication manufactured, distributed, or labeled by ENVIRO SPECIALTY CHEMICALS INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT:

Benzalkonium Chloride 0.13%

PURPOSE:

Antiseptic/Hand & Skin Sanitizer

USES:

Sanitizing Hand Wipes to help decrease bacteria on the skin. Recommended for single use.

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 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 FOR USE:

Wipe liberally over the hands & body, rub into skin until dry. Recommended for single use.

INACTIVE INGREDIENTS:

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Laureth 4, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Questions?

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

SPL UNCLASSIFIED SECTION

KILLS 99.99% OF HARMFUL GERMS

WITH SOOTHING ALOE VERA

LONG-LASTING, ALCOHOL-FREE PROTECTION FROM GERMS

Formulated and enhanced with Zetrisil™

A PROPRIETARY SILICONE QUATERNARY SOLUTION

FAST ACTING 15 SECOND FORMULA

BLEACH FREE

CAUTION

SEE BACK PANEL FOR PRECAUTIONARY STATEMENTS AND FIRST AID

100% LINT FREE

Please dispose of used wipes responsibly.

Do not dispose used wipes down the toilet.

DISTRIBUTED BY: ESC BRANDS, LLC.

664 OLD HARGRAVES ROAD, SUITE B

LEXINGTON NC 27295

888 331-8332

WWW.MY-SHIELD.COM 

FORMULATED IN THE USA

MADE IN CHINA

Packaging

Packaging

Packaging

INGREDIENTS AND APPEARANCE

MY-SHIELD SANITIZING HAND WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-010
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 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
LAURETH-4 (UNII: 6HQ855798J)
POLIHEXANIDE (UNII: 322U039GMF)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-010-20	48 in 1 CASE	11/01/2019
1		20 in 1 POUCH
1		5.25 g in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 71884-010-80	12 in 1 CASE	11/01/2019
2		80 in 1 CONTAINER
2		8.13 g in 1 PATCH; Type 0: Not a Combination Product
3	NDC: 71884-010-76	1 in 1 CASE	02/18/2020
3		80 in 1 JAR
3		15 g in 1 PATCH; Type 0: Not a Combination Product
4	NDC: 71884-010-50	1 in 1 CASE	02/18/2020
4		50 in 1 PACKAGE
4		15.6 g in 1 PATCH; Type 0: Not a Combination Product
5	NDC: 71884-010-82	1 in 1 CASE	02/18/2020
5		200 in 1 PACKAGE
5		16.016 g in 1 PATCH; Type 0: Not a Combination Product
6	NDC: 71884-010-68	1 in 1 CASE	02/18/2020
6		800 in 1 PACKAGE
6		15 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/01/2019

Labeler - ENVIRO SPECIALTY CHEMICALS INC (202621850)