QUICK GUARD- alcohol patch

Quick Guard by

Drug Labeling and Warnings

Quick Guard by is a Otc medication manufactured, distributed, or labeled by Reliance Enterprises USA Inc. DBA - Premier wholesale, Imperial Palace Commodity(Dongguan)CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 75%(v/v)

Purpose

Antiseptic

Uses

For sanitizng and to help reduce bacteria on skin that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in or near eyes
• on open skin wounds or burns

When using this product

Avoid contact with eyes. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

If irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222

Directions

• Apply to hands and skin. No rinsing required. Discard after use.
• Children under 6 years of age should be supervised when using this product.

Other information

• Avoid freezing and store in cool and dry place. Keep away from heat and direct sunlight.
• Dispose of the wipes in trash. Do not flush it into the toilet. May discolor certain fabrics.

Inactive ingredients

Glycerin and Water

Question

Call us toll free at 1-855-22-Premier. Mon-Fri(8am to 5pm EST)

 Principal Display Panel

NDC: 80702-075-80

Quick Guard

Kills Germs

Alcohol Wipes

Gentle and Effectively Cleansing

INGREDIENTS AND APPEARANCE

QUICK GUARD 
alcohol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80702-075
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80702-075-80	80 in 1 BOX	12/01/2020
1		0.75 L 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	part333A	12/01/2020

Labeler - Reliance Enterprises USA Inc. DBA - Premier wholesale (013727384)

Registrant - Reliance Enterprises USA Inc. DBA - Premier wholesale (013727384)

Establishment
Name	Address	ID/FEI	Business Operations
Imperial Palace Commodity(Dongguan)CO.,LTD		544367643	manufacture(80702-075)