MED MATE INSTANT HAND SANITIZER- alcohol gel

MED Mate Instant Hand Sanitizer by

Drug Labeling and Warnings

MED Mate Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by United Specialty Solutions, BLUE CROSS LABORATORIES, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70%. Purpose: Antimicrobial

Purpose

Antimicrobial, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria on the skin that could cause disease

Recommended for repeated use,

Warnings

Flammable. Keep away from heat or flame.

For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes throughly with water.

Stop and ask a doctor if irritation or rash appears and last.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Place a thumbnail size amount in your palm.
• Rub hands together briskly until dry.
• Children under 6 years of age must be supervised when using Med-Made

Inactive ingredients

Water, Glycerin, Propylene Glycol, Aloe Vera, Carbomer, Vitamin E

OTHER SAFETY INFORMATION

Questions or comments?

Call 1-888-760-7018

Package Label - Principal Display Panel

MED MAte

Instant Hand Sanitizer

Fight against 99% of germs, bacteria, and viruses

Made with 70% Ethanol

Made in the U.S.A.

16.9 FL OZ (473mL)

INGREDIENTS AND APPEARANCE

MED MATE INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80263-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80263-001-01	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/25/2020
2	NDC: 80263-001-02	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/25/2020

Labeler - United Specialty Solutions (115068941)

Establishment
Name	Address	ID/FEI	Business Operations
BLUE CROSS LABORATORIES, INC		008298879	manufacture(80263-001)