7T FOAMING ALCOHOL HAND SANITIZER- ethyl alcohol liquid

7T Foaming Alcohol Hand Sanitizer by

Drug Labeling and Warnings

7T Foaming Alcohol Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Avmor. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 70% v/v

Purpose

Antiseptic.

Uses

• Kills harmful bacteria/germs.
• For personal hand hygiene to help prevent the spread of bacteria.

Warnings

• For external use only.
• Flammable, keep away from fire or flame.

When using this product

• Avoid contact with eyes. Should this occur, flush eyes with water.

• If irritation and redness develops.
• If swallowed, call poison control centre or get medical help right away.

Keep out of reach of children

Directions

• Use as needed.
• Apply a minimum of 0.4 ml (0.01 oz) of sanitizer into the palm of your hand. Rub product onto hands for at least 30 seconds and allow to dry.
• For children under 11, use only under adult supervision.

Other Information

• Store in a cool, dry place below 40 °C (104 F)

Inactive Ingredients

• Water (Aqua), 2-propanol, Bis-PEG-12 Dimethicone, Cetyl Alcohol, Denatonium Benzoate

Questions?

950, Michelin, Laval, Quebec,Canada H7L5C11 800 387-8074.   www.avmor.com

PRINCIPAL DISPLAY PANEL

Avmor®

7T FOAMING ALCOHOL HAND SANITIZER

Product certified for reduced environmental impact. View specific attributes evaluated: UL.com/EL

250 ml (8.5 US fl oz)

INGREDIENTS AND APPEARANCE

7T FOAMING ALCOHOL HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63937-2198
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)
CETYL ALCOHOL (UNII: 936JST6JCN)
DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63937-2198-1	12 in 1 BOX	02/20/2020
1		250 mL in 1 BOTTLE; 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	02/18/2020

Labeler - Avmor (202107827)

Establishment
Name	Address	ID/FEI	Business Operations
Avmor		202107827	manufacture(63937-2198) , label(63937-2198) , pack(63937-2198)